A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577076



Internal ID16364485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62039466..62040192hg38UCSC Ensembl
Innerchr18:59706699..59707425hg19UCSC Ensembl
Innerchr18:57857679..57858405hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38727
hg19727
hg18727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5963n54
Supporting Variantsnssv884941, nssv884944, nssv884942, nssv884943
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577076
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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