A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942180



Internal ID21362249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10674409..10674493hg38UCSC Ensembl
chr8:10531919..10532003hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15199291
SamplesHG002
Known GenesC8orf74
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3942180
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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