A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13939561



Internal ID3941377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112766318..112767228hg38UCSC Ensembl
Innerchr10:112766337..112767210hg38UCSC Ensembl
Outerchr10:112766300..112767247hg38UCSC Ensembl
chr10:114526077..114526987hg19UCSC Ensembl
Innerchr10:114526096..114526969hg19UCSC Ensembl
Outerchr10:114526059..114527006hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624587
Supporting Variants
SamplesNA18966
Known GenesVTI1A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13939561
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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