A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577669



Internal ID16365078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76392971..76394721hg38UCSC Ensembl
Innerchr18:74104927..74106677hg19UCSC Ensembl
Innerchr18:72233915..72235665hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381751
hg191751
hg181751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6071n54
Supporting Variantsnssv887406, nssv887405
Samples
Known GenesZNF516
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577669
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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