A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058535



Internal ID19147754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71535310..71599178hg38UCSC Ensembl
Innerchr18:69202546..69266414hg19UCSC Ensembl
Innerchr18:67353526..67417394hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3863869
hg1963869
hg1863869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562972, nssv3562971, nssv3562973
Samples
Known GenesLOC100505776
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058535
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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