A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104264



Internal ID20671304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97957677..97960269hg38UCSC Ensembl
chr3:97676521..97679113hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg382593
hg192593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359431
Supporting Variants
Samples
Known GenesMINA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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