A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525933



Internal ID8420208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31113428..31174468hg38UCSC Ensembl
Innerchr6:31081205..31142245hg19UCSC Ensembl
Innerchr6:31189184..31250224hg18UCSC Ensembl
Innerchr6:31189184..31250224hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3861041
hg1961041
hg1861041
hg1761041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702139
Samples
Known GenesCCHCR1, CDSN, POU5F1, PSORS1C1, PSORS1C2, PSORS1C3, TCF19
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525933
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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