A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335855



Internal ID20993408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47314478..47366392hg38UCSC Ensembl
chr2:47541617..47593531hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3851915
hg1951915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3853n223
Supporting Variantsnssv18089394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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