A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705020



Internal ID15094986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29611735..29612148hg38UCSC Ensembl
Innerchr10:29900664..29901077hg19UCSC Ensembl
Innerchr10:29940670..29941083hg18UCSC Ensembl
Innerchr10:29940670..29941083hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38414
hg19414
hg18414
hg17414
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528427
Supporting Variants
Samples
Known GenesSVIL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705020
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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