A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980451



Internal ID20547491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119723614..119724237hg38UCSC Ensembl
chr10:121483126..121483749hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454337
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980451
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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