A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984351



Internal ID20551391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77947218..77950393hg38UCSC Ensembl
chr10:79706976..79710151hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg383176
hg193176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455014
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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