A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978653



Internal ID20545693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125805997..125811138hg38UCSC Ensembl
chr10:127494566..127499707hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385142
hg195142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442526
Supporting Variants
Samples
Known GenesUROS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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