A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690850



Internal ID18989131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24849050..24906804hg38UCSC Ensembl
Innerchr9:24849048..24906802hg19UCSC Ensembl
Innerchr9:24839048..24896802hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3857755
hg1957755
hg1857755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029043
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)nssv3690850
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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