A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199291



Internal ID21338087
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3942180
Supporting Variants
SamplesHG002
Known GenesC8orf74
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199291
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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