A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13664079



Internal ID641972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73560..74551hg38UCSC Ensembl
Innerchr10:73583..74528hg38UCSC Ensembl
Outerchr10:73537..74574hg38UCSC Ensembl
chr10:119500..120491hg19UCSC Ensembl
Innerchr10:119523..120468hg19UCSC Ensembl
Outerchr10:119477..120514hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622067
Supporting Variants
SamplesHG00281
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13664079
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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