A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342980



Internal ID21000533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:182867156..182870301hg38UCSC Ensembl
chr2:183731884..183735029hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg383146
hg193146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081634
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342980
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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