A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525985



Internal ID15106592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:70018310..70056612hg38UCSC Ensembl
Innerchr6:70728202..70766504hg19UCSC Ensembl
Innerchr6:70784923..70823225hg18UCSC Ensembl
Innerchr6:70784923..70823225hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3838303
hg1938303
hg1838303
hg1738303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702205
Samples
Known GenesCOL19A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525985
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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