A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577634



Internal ID16365043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73056263..73059001hg38UCSC Ensembl
Innerchr18:70723498..70726236hg19UCSC Ensembl
Innerchr18:68874478..68877216hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg382739
hg192739
hg182739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6067n54
Supporting Variantsnssv887321, nssv887320, nssv887325, nssv887319, nssv887324, nssv887323, nssv887322
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577634
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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