A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624687



Internal ID7011537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118321858..118325333hg38UCSC Ensembl
Innerchr10:118321858..118325333hg38UCSC Ensembl
Outerchr10:118321837..118325462hg38UCSC Ensembl
chr10:120081370..120084845hg19UCSC Ensembl
Innerchr10:120081370..120084845hg19UCSC Ensembl
Outerchr10:120081349..120084974hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383476
hg193476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946601
SamplesHG03583
Known GenesFAM204A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624687
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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