A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046122



Internal ID20613162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2867087..2895902hg38UCSC Ensembl
chr19:2867085..2895900hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3828816
hg1928816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519396
Supporting Variants
Samples
Known GenesZNF556
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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