A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956434



Internal ID22731620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50301101..50301197hg38UCSC Ensembl
chr20:48917638..48917734hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406198
Samples
Known GenesLOC284751
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956434
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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