A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577314



Internal ID16364723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67588936..68015626hg38UCSC Ensembl
Innerchr18:65256173..65682863hg19UCSC Ensembl
Innerchr18:63407153..63833843hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38426691
hg19426691
hg18426691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv886386
Samples
Known GenesLOC643542
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577314
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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