A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723239



Internal ID19021520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:77295805..77527724hg38UCSC Ensembl
Innerchr18:75007761..75239680hg19UCSC Ensembl
Innerchr18:73136749..73368668hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38231920
hg19231920
hg18231920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058599
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3723239
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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