A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624678



Internal ID7011528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117394730..117395658hg38UCSC Ensembl
Innerchr10:117394747..117395641hg38UCSC Ensembl
Outerchr10:117394713..117395675hg38UCSC Ensembl
chr10:119154241..119155169hg19UCSC Ensembl
Innerchr10:119154258..119155152hg19UCSC Ensembl
Outerchr10:119154224..119155186hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946487, essv13946486
SamplesNA18953, NA19063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624678
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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