A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526876



Internal ID15454169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155134413..155141603hg38UCSC Ensembl
Innerchr4:156055565..156062755hg19UCSC Ensembl
Innerchr4:156275015..156282205hg18UCSC Ensembl
Innerchr4:156413170..156420360hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg387191
hg197191
hg187191
hg177191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703234
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526876
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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