A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702854



Internal ID15092820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8011813..8024215hg38UCSC Ensembl
Innerchr10:8053776..8066178hg19UCSC Ensembl
Innerchr10:8093782..8106184hg18UCSC Ensembl
Innerchr10:8093782..8106184hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3812403
hg1912403
hg1812403
hg1712403
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526540
Supporting Variants
Samples
Known GenesTAF3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702854
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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