A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165733



Internal ID20732773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133190676..133195101hg38UCSC Ensembl
chr8:134202919..134207344hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg384426
hg194426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430593
Supporting Variants
Samples
Known GenesWISP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165733
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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