A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072338



Internal ID20639378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38376137..38380092hg38UCSC Ensembl
chr21:39748059..39752014hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg383956
hg193956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544173
Supporting Variants
Samples
Known GenesERG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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