A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044986



Internal ID20612026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11254396..11254692hg38UCSC Ensembl
chr19:11365072..11365368hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521465
Supporting Variants
Samples
Known GenesDOCK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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