A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577633



Internal ID16365042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73056263..73058765hg38UCSC Ensembl
Innerchr18:70723498..70726000hg19UCSC Ensembl
Innerchr18:68874478..68876980hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg382503
hg192503
hg182503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6067n54
Supporting Variantsnssv887315, nssv887316, nssv887317, nssv887318
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577633
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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