A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172174



Internal ID20739214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:82356734..82415686hg38UCSC Ensembl
chr8:83268969..83327921hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3858953
hg1958953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420307
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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