A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527084



Internal ID15454377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:36996856..37003956hg38UCSC Ensembl
Innerchr4:36998478..37005578hg19UCSC Ensembl
Innerchr4:36674873..36681973hg18UCSC Ensembl
Innerchr4:36821044..36828144hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg387101
hg197101
hg187101
hg177101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703463
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527084
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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