A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398579



Internal ID22456449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9765556..9765874hg38UCSC Ensembl
chr4_gl000193_random:32870..33188hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398579
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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