A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346865



Internal ID21004418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44850463..44879125hg38UCSC Ensembl
chr2:45077602..45106264hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3828663
hg1928663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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