A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525003



Internal ID15452296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:48101030..48101138hg38UCSC Ensembl
Innerchr6:48068766..48068874hg19UCSC Ensembl
Innerchr6:48176725..48176833hg18UCSC Ensembl
Innerchr6:48176725..48176833hg17UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38109
hg19109
hg18109
hg17109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701037
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525003
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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