A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528130



Internal ID15455423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45088349..45116229hg38UCSC Ensembl
Innerchr6:45056086..45083966hg19UCSC Ensembl
Innerchr6:45164064..45191944hg18UCSC Ensembl
Innerchr6:45164064..45191944hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3827881
hg1927881
hg1827881
hg1727881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704675
Samples
Known GenesSUPT3H
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528130
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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