A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528116



Internal ID15108723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17989134..17993498hg38UCSC Ensembl
Innerchr10:18278063..18282427hg19UCSC Ensembl
Innerchr10:18318069..18322433hg18UCSC Ensembl
Innerchr10:18318069..18322433hg17UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg384365
hg194365
hg184365
hg174365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704659
Samples
Known GenesSLC39A12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528116
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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