A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047931



Internal ID20614971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40223625..40229348hg38UCSC Ensembl
chr19:40729532..40735255hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385724
hg195724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521731
Supporting Variants
Samples
Known GenesCNTD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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