A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525566



Internal ID15106173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:7733826..7735555hg38UCSC Ensembl
Innerchr6:7734059..7735788hg19UCSC Ensembl
Innerchr6:7679058..7680787hg18UCSC Ensembl
Innerchr6:7679058..7680787hg17UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg381730
hg191730
hg181730
hg171730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701705
Samples
Known GenesBMP6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525566
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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