A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984047



Internal ID20551087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75228..88957hg38UCSC Ensembl
chr10:121168..134897hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3813730
hg1913730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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