A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527719



Internal ID15455012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:109303734..109310406hg38UCSC Ensembl
Innerchr6:109624937..109631609hg19UCSC Ensembl
Innerchr6:109731630..109738302hg18UCSC Ensembl
Innerchr6:109731630..109738302hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386673
hg196673
hg186673
hg176673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704200
Samples
Known GenesCCDC162P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527719
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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