A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878868



Internal ID16172824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29134027..29185688hg38UCSC Ensembl
Innerchr18:26713991..26765653hg19UCSC Ensembl
Innerchr18:24967989..25019651hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3851662
hg1951663
hg1851663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576593
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878868
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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