A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173499



Internal ID20740539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92914201..92915000hg38UCSC Ensembl
chr8:93926429..93927228hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420421
Supporting Variants
Samples
Known GenesTRIQK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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