A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167761



Internal ID20734801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48739870..48775038hg38UCSC Ensembl
chr8:49652429..49687597hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3835169
hg1935169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167761
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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