A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691214



Internal ID18989495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1003739..1033354hg38UCSC Ensembl
Innerchr9:1003739..1033354hg19UCSC Ensembl
Innerchr9:993739..1023354hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3829616
hg1929616
hg1829616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022798
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)nssv3691214
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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