A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152580



Internal ID15880951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3428129..3449382hg38UCSC Ensembl
Innerchr4:3429856..3451109hg19UCSC Ensembl
Innerchr4:3399654..3420907hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3821254
hg1921254
hg1821254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593457
Supporting Variants
SamplesNINDS_51
Known GenesHGFAC, RGS12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152580
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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