A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690157



Internal ID18988438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39445501..39833345hg38UCSC Ensembl
Innerchr9:41475094..41978363hg19UCSC Ensembl
Innerchr9:41465094..41968363hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38387845
hg19503270
hg18503270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023869
Supporting Variants
Samples
Known GenesKGFLP2, LOC653501, MGC21881, SPATA31A5, SPATA31A7, ZNF658B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690157
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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