A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046597



Internal ID20613637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3685501..3694100hg38UCSC Ensembl
chr19:3685499..3694098hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388600
hg198600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516719
Supporting Variants
Samples
Known GenesPIP5K1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046597
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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