A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614550



Internal ID16055273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68959841..69228107hg38UCSC Ensembl
Innerchr9:71574757..71843023hg19UCSC Ensembl
Innerchr9:70764577..71032843hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38268267
hg19268267
hg18268267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176361
Samples1798860277_A
Known GenesFXN, PIP5K1B, PRKACG, TJP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614550
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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