A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353941



Internal ID21011494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174966470..174967379hg38UCSC Ensembl
chr2:175831198..175832107hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38910
hg19910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081406
Samples
Known GenesCHN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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