A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv996674



Internal ID15943944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40681959..40776145hg38UCSC Ensembl
Innerchr4:40683976..40778162hg19UCSC Ensembl
Innerchr4:40378733..40472919hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3894187
hg1994187
hg1894187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594053
Supporting Variants
Samples
Known GenesNSUN7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv996674
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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