A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690237



Internal ID18988518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39456483..39833345hg38UCSC Ensembl
Innerchr9:41601501..41978363hg19UCSC Ensembl
Innerchr9:41591501..41968363hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38376863
hg19376863
hg18376863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033141
Supporting Variants
Samples
Known GenesKGFLP2, LOC653501, MGC21881
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690237
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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