A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623127



Internal ID7009984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46159786..46227801hg38UCSC Ensembl
chr10:47531022..47599037hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3868016
hg1968016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv120e214
Supporting Variantsessv13785576, essv13785581, essv13785577, essv13785579, essv13785573, essv13785582, essv13785580, essv13785578, essv13785574, essv13785575
SamplesHG03548, HG00315, NA18940, HG03385, HG03490, NA12275, HG00290, HG02309, HG01444, HG01269
Known GenesANTXRLP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623127
Frequency
Sample Size2504
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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