A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614291



Internal ID16401700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39440753..39444669hg38UCSC Ensembl
Innerchr9:39440752..39444668hg19UCSC Ensembl
Innerchr9:39430752..39434668hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg383917
hg193917
hg183917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134086
Samples
Known GenesLOC653501, ZNF658B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614291
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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