A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614302



Internal ID16401711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60995957..61002943hg38UCSC Ensembl
Innerchr9:39966453..39973432hg19UCSC Ensembl
Innerchr9:39956453..39963432hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg386987
hg196980
hg186980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12694n54
Supporting Variantsnssv1134118
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614302
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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