A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525297



Internal ID15452590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194811713..194812741hg38UCSC Ensembl
Innerchr3:194532442..194533470hg19UCSC Ensembl
Innerchr3:196013731..196014759hg18UCSC Ensembl
Innerchr3:196013739..196014767hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381029
hg191029
hg181029
hg171029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701403
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525297
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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