A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346051



Internal ID21003604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:199988801..200022000hg38UCSC Ensembl
chr2:200853524..200886723hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3833200
hg1933200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4254n223
Supporting Variantsnssv18083967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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