A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017837



Internal ID19107054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31568872..31620107hg38UCSC Ensembl
Innerchr9:31568870..31620105hg19UCSC Ensembl
Innerchr9:31558870..31610105hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3851236
hg1951236
hg1851236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688856
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)nsv1017837
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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