A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622098



Internal ID6662268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1188986..1190395hg38UCSC Ensembl
Innerchr10:1188987..1190394hg38UCSC Ensembl
Outerchr10:1188985..1190396hg38UCSC Ensembl
chr10:1234926..1236335hg19UCSC Ensembl
Innerchr10:1234927..1236334hg19UCSC Ensembl
Outerchr10:1234925..1236336hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381410
hg191410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13664679, essv13664708, essv13664698, essv13664691, essv13664682, essv13664700, essv13664677, essv13664697, essv13664687, essv13664706, essv13664689, essv13664678, essv13664696, essv13664693, essv13664701, essv13664688, essv13664707, essv13664686, essv13664709, essv13664680, essv13664676, essv13664684, essv13664683, essv13664695, essv13664703, essv13664705, essv13664704, essv13664694, essv13664692, essv13664699, essv13664690, essv13664681, essv13664685, essv13664702
SamplesNA20351, HG03382, NA19401, HG03055, HG02419, NA19435, HG03046, HG03124, HG02944, NA18865, NA19017, HG03268, NA18868, NA19143, HG02836, HG03470, HG02568, HG02643, HG03100, HG01747, HG03169, HG02922, HG02623, HG02938, HG02571, NA19307, HG03028, NA19921, NA19116, NA19431, HG02891, HG03060, NA19350, NA19385
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622098
Frequency
Sample Size2504
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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