A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576275



Internal ID16363684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1757522..1865219hg38UCSC Ensembl
Innerchr18:1757523..1865220hg19UCSC Ensembl
Innerchr18:1747523..1855220hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38107698
hg19107698
hg18107698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5813n54
Supporting Variantsnssv877335
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576275
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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