A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056737



Internal ID19145956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29758384..29807099hg38UCSC Ensembl
Innerchr18:27338349..27387064hg19UCSC Ensembl
Innerchr18:25592347..25641062hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3848716
hg1948716
hg1848716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564152
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)nsv1056737
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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