A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622898



Internal ID7009756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35406118..35410277hg38UCSC Ensembl
Innerchr10:35406149..35410246hg38UCSC Ensembl
Outerchr10:35406087..35410308hg38UCSC Ensembl
chr10:35695046..35699205hg19UCSC Ensembl
Innerchr10:35695077..35699174hg19UCSC Ensembl
Outerchr10:35695015..35699236hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384160
hg194160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13752234, essv13752233, essv13752236, essv13752235
SamplesHG02952, HG03460, HG02314, NA19713
Known GenesCCNY
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622898
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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