A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576318



Internal ID16017041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4330954..4335455hg38UCSC Ensembl
Innerchr18:4330954..4335455hg19UCSC Ensembl
Innerchr18:4320954..4325455hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg384502
hg194502
hg184502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150584
SamplesHGDP00462
Known GenesDLGAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576318
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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