A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614546



Internal ID16055269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68428973..68703901hg38UCSC Ensembl
Innerchr9:71043889..71318817hg19UCSC Ensembl
Innerchr9:70233709..70508637hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38274929
hg19274929
hg18274929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134760
Samples
Known GenesLOC101927015, PGM5, TMEM252
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614546
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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