A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543949



Internal ID20917190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49236388..49238609hg38UCSC Ensembl
chr20:47852925..47855146hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg382222
hg192222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068983
Samples
Known GenesDDX27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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