A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522826



Internal ID15450119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:61458592..61463697hg38UCSC Ensembl
Innerchr5:60754419..60759524hg19UCSC Ensembl
Innerchr5:60790176..60795281hg18UCSC Ensembl
Innerchr5:60790176..60795281hg17UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg385106
hg195106
hg185106
hg175106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698476
Samples
Known GenesZSWIM6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522826
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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