A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340890



Internal ID20998443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47251741..47339043hg38UCSC Ensembl
chr2:47478880..47566182hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3887303
hg1987303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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