A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044984



Internal ID20612024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11230401..11233600hg38UCSC Ensembl
chr19:11341077..11344276hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517265
Supporting Variants
Samples
Known GenesDOCK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044984
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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