A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152950



Internal ID15880263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130041108..130082450hg38UCSC Ensembl
Innerchr4:130962263..131003605hg19UCSC Ensembl
Innerchr4:131181713..131223055hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3841343
hg1941343
hg1841343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595413
Supporting Variants
SamplesNINDS_183
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152950
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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