A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403599



Internal ID22461469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39309045..39309695hg38UCSC Ensembl
chr21:40680971..40681621hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958317
Supporting Variants
Samples
Known GenesBRWD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403599
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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