A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199038



Internal ID20766078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7768415..7825056hg38UCSC Ensembl
chr19:7833301..7889942hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3856642
hg1956642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532645
Supporting Variants
Samples
Known GenesCLEC4GP1, CLEC4M
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199038
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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