A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980510



Internal ID20547550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120845362..120850520hg38UCSC Ensembl
chr10:122604874..122610032hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg385159
hg195159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448342
Supporting Variants
Samples
Known GenesMIR5694, WDR11-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980510
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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