A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577070



Internal ID16364479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60605580..60649293hg38UCSC Ensembl
Innerchr18:58272813..58316526hg19UCSC Ensembl
Innerchr18:56423793..56467506hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3843714
hg1943714
hg1843714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5961n54
Supporting Variantsnssv1149824
Samples1782681110_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577070
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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