A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690554



Internal ID18988835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12014484..12101436hg38UCSC Ensembl
Innerchr9:12014484..12101436hg19UCSC Ensembl
Innerchr9:12004484..12091436hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3886953
hg1986953
hg1886953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016397
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)nssv3690554
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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