A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640444



Internal ID21832491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9616900..9618663hg38UCSC Ensembl
chr15:20022212..20024077hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381764
hg191866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045195
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640444
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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