A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199578



Internal ID20766618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48420718..48421320hg38UCSC Ensembl
chr19:48923975..48924577hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523240
Supporting Variants
Samples
Known GenesGRIN2D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199578
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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