A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698728



Internal ID15435380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172652886..172728004hg38UCSC Ensembl
Innerchr5:172079889..172155007hg19UCSC Ensembl
Innerchr5:172012494..172087612hg18UCSC Ensembl
Innerchr5:172012494..172087612hg17UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3875119
hg1975119
hg1875119
hg1775119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523045
Supporting Variants
Samples
Known GenesNEURL1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698728
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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