A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016067



Internal ID19105285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22210875..22432655hg38UCSC Ensembl
Innerchr9:22210874..22432654hg19UCSC Ensembl
Innerchr9:22200874..22422654hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38221781
hg19221781
hg18221781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690723
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)nsv1016067
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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