A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525377



Internal ID15452670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4568948..4572143hg38UCSC Ensembl
Innerchr6:4569182..4572377hg19UCSC Ensembl
Innerchr6:4514181..4517376hg18UCSC Ensembl
Innerchr6:4514181..4517376hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg383196
hg193196
hg183196
hg173196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701498
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525377
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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