A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058214



Internal ID18800745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31394649..31473928hg38UCSC Ensembl
Innerchr18:28974612..29053891hg19UCSC Ensembl
Innerchr18:27228610..27307889hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3879280
hg1979280
hg1879280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3328n100
Supporting Variantsnssv3564160
Samples
Known GenesDSG3, DSG4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058214
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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