A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524213



Internal ID15104820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:38139068..38192851hg38UCSC Ensembl
Innerchr6:38106844..38160627hg19UCSC Ensembl
Innerchr6:38214822..38268605hg18UCSC Ensembl
Innerchr6:38214822..38268605hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3853784
hg1953784
hg1853784
hg1753784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700100
Samples
Known GenesBTBD9, ZFAND3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524213
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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