A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614551



Internal ID16055274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68997975..69056200hg38UCSC Ensembl
Innerchr9:71612891..71671116hg19UCSC Ensembl
Innerchr9:70802711..70860936hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3858226
hg1958226
hg1858226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134763
Samples
Known GenesFXN, PIP5K1B, PRKACG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614551
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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