A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688786



Internal ID18987067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29951546..30249260hg38UCSC Ensembl
Innerchr9:29951544..30249258hg19UCSC Ensembl
Innerchr9:29941544..30239258hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38297715
hg19297715
hg18297715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022833
Supporting Variants
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)nssv3688786
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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