A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526406



Internal ID15453699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:139943672..139949481hg38UCSC Ensembl
Innerchr5:139323257..139329066hg19UCSC Ensembl
Innerchr5:139303441..139309250hg18UCSC Ensembl
Innerchr5:139303441..139309250hg17UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg385810
hg195810
hg185810
hg175810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702706
Samples
Known GenesNRG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526406
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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