A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170965



Internal ID20738005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87427682..87595042hg38UCSC Ensembl
chr8:88439910..88607270hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38167361
hg19167361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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