A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344568



Internal ID21002121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6053554..6058243hg38UCSC Ensembl
chr2:6193686..6198375hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg384690
hg194690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344568
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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