A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13946601



Internal ID3931009
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624687
Supporting Variants
SamplesHG03583
Known GenesFAM204A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13946601
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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