A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152953



Internal ID15855144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131025220..131426734hg38UCSC Ensembl
Innerchr4:131946375..132347889hg19UCSC Ensembl
Innerchr4:132165825..132567339hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38401515
hg19401515
hg18401515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595426
Supporting Variants
Samples1780862457_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152953
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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