A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339951



Internal ID20997504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216142349..216145842hg38UCSC Ensembl
chr2:217007072..217010565hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg383494
hg193494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085755
Samples
Known GenesXRCC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339951
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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