A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343281



Internal ID21000834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215955392..215959269hg38UCSC Ensembl
chr2:216820115..216823992hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg383878
hg193878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085749
Samples
Known GenesMREG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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