A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577822



Internal ID16018545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78980137..78980976hg38UCSC Ensembl
Innerchr18:76740137..76740976hg19UCSC Ensembl
Innerchr18:74841125..74841964hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38840
hg19840
hg18840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6103n54
Supporting Variantsnssv888908
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577822
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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