A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392714



Internal ID22450584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9951166..9951258hg38UCSC Ensembl
chr21:10429194..10429286hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5949907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392714
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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