A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576542



Internal ID16363951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14913293..14978678hg38UCSC Ensembl
Innerchr18:14913292..14978677hg19UCSC Ensembl
Innerchr18:14903292..14968677hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3865386
hg1965386
hg1865386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878460
Samples
Known GenesLOC400644
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576542
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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