A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697015



Internal ID15433667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:75639073..75640379hg38UCSC Ensembl
Innerchr18:73351028..73352334hg19UCSC Ensembl
Innerchr18:71480016..71481322hg18UCSC Ensembl
Innerchr18:71480016..71481322hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381307
hg191307
hg181307
hg171307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519728
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697015
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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