A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524116



Internal ID15451409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181087652..181138125hg38UCSC Ensembl
Innerchr5:180514652..180565125hg19UCSC Ensembl
Innerchr5:180447258..180497731hg18UCSC Ensembl
Innerchr5:180447258..180497731hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3850474
hg1950474
hg1850474
hg1750474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv365n21
Supporting Variantsnssv699994
Samples
Known GenesOR2V1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524116
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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