A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977682



Internal ID20544722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11402616..11422802hg38UCSC Ensembl
chr10:11444615..11464801hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3820187
hg1920187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450624
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977682
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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