A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577682



Internal ID16365091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76393499..76395964hg38UCSC Ensembl
Innerchr18:74105455..74107920hg19UCSC Ensembl
Innerchr18:72234443..72236908hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg382466
hg192466
hg182466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6075n54
Supporting Variantsnssv887534
Samples
Known GenesZNF516
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577682
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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