A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022833



Internal ID19112051
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 StatusM
Merged Variants
Supporting Variantsnssv3688786
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)nsv1022833
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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