A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518956



Internal ID20892317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6756450..6757152hg38UCSC Ensembl
chr19:6756461..6757163hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049683
Samples
Known GenesSH2D3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518956
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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