A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071983



Internal ID20639023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33652036..33653059hg38UCSC Ensembl
chr21:35024342..35025365hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381024
hg191024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546663
Supporting Variants
Samples
Known GenesITSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00209


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