A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021539



Internal ID19110757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39459144..39990996hg38UCSC Ensembl
Innerchr9:41604162..42136014hg19UCSC Ensembl
Innerchr9:41594162..42126014hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38531853
hg19531853
hg18531853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690239
Samples
Known GenesKGFLP2, LOC643648, 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)nsv1021539
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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