A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978657



Internal ID20545697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125980071..125985993hg38UCSC Ensembl
chr10:127668640..127674562hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg385923
hg195923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450165
Supporting Variants
Samples
Known GenesFANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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