A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980442



Internal ID20547482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119623744..119624511hg38UCSC Ensembl
chr10:121383256..121384023hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441882
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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