A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528588



Internal ID15455881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149082333..149088724hg38UCSC Ensembl
Innerchr6:149403469..149409860hg19UCSC Ensembl
Innerchr6:149445162..149451553hg18UCSC Ensembl
Innerchr6:149445162..149451553hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg386392
hg196392
hg186392
hg176392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705213
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528588
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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