A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527906



Internal ID15455199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73759137..73765324hg38UCSC Ensembl
Innerchr6:74468860..74475047hg19UCSC Ensembl
Innerchr6:74525581..74531768hg18UCSC Ensembl
Innerchr6:74525581..74531768hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg386188
hg196188
hg186188
hg176188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704412
Samples
Known GenesCD109
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527906
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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