A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525235



Internal ID15452528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153193876..153252310hg38UCSC Ensembl
Innerchr6:153515011..153573445hg19UCSC Ensembl
Innerchr6:153556704..153615138hg18UCSC Ensembl
Innerchr6:153607125..153665559hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3858435
hg1958435
hg1858435
hg1758435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701325
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525235
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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