A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045978



Internal ID20613018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1915701..1951100hg38UCSC Ensembl
chr19:1915700..1951099hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3835400
hg1935400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535405
Supporting Variants
Samples
Known GenesCSNK1G2, SCAMP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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