A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016152



Internal ID19105370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23073757..23361807hg38UCSC Ensembl
Innerchr9:23073756..23361805hg19UCSC Ensembl
Innerchr9:23063756..23351805hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38288051
hg19288050
hg18288050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690732
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)nsv1016152
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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