A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520134



Internal ID15447427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149088724..149088996hg38UCSC Ensembl
Innerchr6:149409860..149410132hg19UCSC Ensembl
Innerchr6:149451553..149451825hg18UCSC Ensembl
Innerchr6:149451553..149451825hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38273
hg19273
hg18273
hg17273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661082, nssv685310
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520134
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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