A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978024



Internal ID20545064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124776577..124781312hg38UCSC Ensembl
chr10:126465146..126469881hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384736
hg194736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454703
Supporting Variants
Samples
Known GenesMETTL10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978024
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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