A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049383



Internal ID20616424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7778105..7791072hg38UCSC Ensembl
chr19:7842991..7855958hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812968
hg1912968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523679
Supporting Variants
Samples
Known GenesCLEC4GP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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