A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701267



Internal ID15437919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56277732..56323877hg38UCSC Ensembl
Innerchr10:58037493..58083638hg19UCSC Ensembl
Innerchr10:57707499..57753644hg18UCSC Ensembl
Innerchr10:57707499..57753644hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3846146
hg1946146
hg1846146
hg1746146
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525189
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701267
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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