A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614323



Internal ID16401732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66791121..66955365hg38UCSC Ensembl
Innerchr9:40737476..40901750hg19UCSC Ensembl
Innerchr9:40727476..40891750hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38164245
hg19164275
hg18164275
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134153, nssv1134154
Samples
Known GenesZNF658
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614323
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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