A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3563035



Internal ID18861316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76695215..76766320hg38UCSC Ensembl
Innerchr18:74407171..74478276hg19UCSC Ensembl
Innerchr18:72536159..72607264hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3871106
hg1971106
hg1871106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061460
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)nssv3563035
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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