A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524630



Internal ID15105237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:88654919..88708284hg38UCSC Ensembl
Innerchr5:87950737..88004101hg19UCSC Ensembl
Innerchr5:87986493..88039857hg18UCSC Ensembl
Innerchr5:87986493..88039857hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3853366
hg1953365
hg1853365
hg1753365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700593
Samples
Known GenesLINC00461, MIR9-2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524630
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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