A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699673



Internal ID15436325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18544350..18586798hg38UCSC Ensembl
Innerchr5:18544459..18586907hg19UCSC Ensembl
Innerchr5:18580216..18622664hg18UCSC Ensembl
Innerchr5:18580216..18622664hg17UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3842449
hg1942449
hg1842449
hg1742449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516047
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699673
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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