A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046069



Internal ID20613109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2692101..2694300hg38UCSC Ensembl
chr19:2692099..2694298hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524062
Supporting Variants
Samples
Known GenesGNG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0013


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