A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577744



Internal ID16365153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78502624..78529783hg38UCSC Ensembl
Innerchr18:76262624..76289783hg19UCSC Ensembl
Innerchr18:74363612..74390771hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3827160
hg1927160
hg1827160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv888588, nssv888589
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577744
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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