A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690703



Internal ID18988984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20638975..20653461hg38UCSC Ensembl
Innerchr9:20638974..20653460hg19UCSC Ensembl
Innerchr9:20628974..20643460hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3814487
hg1914487
hg1814487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019915
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)nssv3690703
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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