A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577287



Internal ID16364696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67104854..67111881hg38UCSC Ensembl
Innerchr18:64772091..64779118hg19UCSC Ensembl
Innerchr18:62923071..62930098hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg387028
hg197028
hg187028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6005n54
Supporting Variantsnssv886253, nssv886255, nssv886254
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577287
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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