A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152674



Internal ID15534184
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
SamplesNINDS_41
Known GenesNSUN7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152674
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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