A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692396



Internal ID18990677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4903709..4947510hg38UCSC Ensembl
Innerchr9:4903709..4947510hg19UCSC Ensembl
Innerchr9:4893709..4937510hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3843802
hg1943802
hg1843802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032013
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)nssv3692396
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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