A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948271



Internal ID22723759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34217756..34218840hg38UCSC Ensembl
chr20:32805562..32806646hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381085
hg191085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394497
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948271
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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