A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577767



Internal ID16365176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78777584..78798607hg38UCSC Ensembl
Innerchr18:76537584..76558607hg19UCSC Ensembl
Innerchr18:74638572..74659595hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3821024
hg1921024
hg1821024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv888728
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577767
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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