A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171804



Internal ID20738844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94571240..94582685hg38UCSC Ensembl
chr8:95583468..95594913hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3811446
hg1911446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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