A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517932



Internal ID15098539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160808118..160862611hg38UCSC Ensembl
Innerchr5:160235125..160289618hg19UCSC Ensembl
Innerchr5:160167703..160222196hg18UCSC Ensembl
Innerchr5:160167703..160222196hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3854494
hg1954494
hg1854494
hg1754494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695344
Samples
Known GenesATP10B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517932
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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