A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623061



Internal ID7009918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44313115..44315156hg38UCSC Ensembl
Innerchr10:44313115..44315156hg38UCSC Ensembl
Outerchr10:44312831..44315391hg38UCSC Ensembl
chr10:44808563..44810604hg19UCSC Ensembl
Innerchr10:44808563..44810604hg19UCSC Ensembl
Outerchr10:44808279..44810839hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382042
hg192042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764992, essv13764993, essv13764991, essv13764996, essv13764998, essv13764995, essv13764997, essv13764994, essv13764990, essv13764999
SamplesHG01173, NA07347, HG00311, HG01628, HG00323, NA20800, HG02554, NA06989, HG00280, HG00343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623061
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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