A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167002



Internal ID20734042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42842701..42843100hg38UCSC Ensembl
chr8:42697844..42698243hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420318
Supporting Variants
Samples
Known GenesTHAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08486


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