A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577793



Internal ID16018516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78951024..79022312hg38UCSC Ensembl
Innerchr18:76711024..76782312hg19UCSC Ensembl
Innerchr18:74812012..74883300hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3871289
hg1971289
hg1871289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150023
Samples1780862415_A
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577793
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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