A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564217



Internal ID18862498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39360269..39454225hg38UCSC Ensembl
Innerchr18:36940233..37034189hg19UCSC Ensembl
Innerchr18:35194231..35288187hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3893957
hg1993957
hg1893957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063320
Supporting Variants
Samples
Known GenesLINC00669
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564217
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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