A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016382



Internal ID20583422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98794378..98795054hg38UCSC Ensembl
chr13:99446632..99447308hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488228
Supporting Variants
Samples
Known GenesDOCK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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