A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577967



Internal ID16018690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:77831304..77831779hg19UCSC Ensembl
Innerchr18:75932292..75932767hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg19476
hg18476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6130n54
Supporting Variantsnssv890319, nssv890320, nssv890318
Samples
Known GenesRBFADN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577967
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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