A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963740



Internal ID22738675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44697736..44708914hg38UCSC Ensembl
chr20:43326377..43337555hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3811179
hg1911179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405661
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963740
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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