A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017031



Internal ID16310987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176417484..176439518hg38UCSC Ensembl
Innerchr4:177338635..177360669hg19UCSC Ensembl
Innerchr4:177575629..177597663hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3822035
hg1922035
hg1822035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596265
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1017031
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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