A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528148



Internal ID15455441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73759137..73783709hg38UCSC Ensembl
Innerchr6:74468860..74493432hg19UCSC Ensembl
Innerchr6:74525581..74550153hg18UCSC Ensembl
Innerchr6:74525581..74550153hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3824573
hg1924573
hg1824573
hg1724573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704695
Samples
Known GenesCD109
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528148
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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