A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515601



Internal ID15443212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40036301..40061443hg38UCSC Ensembl
Innerchr6:40004040..40029182hg19UCSC Ensembl
Innerchr6:40112018..40137160hg18UCSC Ensembl
Innerchr6:40112018..40137160hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3825143
hg1925143
hg1825143
hg1725143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664048, nssv657852, nssv679717, nssv658337, nssv684171, nssv656266, nssv692858, nssv686821
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515601
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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