A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016727



Internal ID19105944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26265536..26434484hg38UCSC Ensembl
Innerchr9:26265534..26434482hg19UCSC Ensembl
Innerchr9:26255534..26424482hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38168949
hg19168949
hg18168949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7484n100
Supporting Variantsnssv3691995
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016727
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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