A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526648



Internal ID15107255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:382254..385899hg38UCSC Ensembl
Innerchr5:382369..386014hg19UCSC Ensembl
Innerchr5:435369..439014hg18UCSC Ensembl
Innerchr5:435369..439014hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg383646
hg193646
hg183646
hg173646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702974
Samples
Known GenesAHRR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526648
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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