A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979678



Internal ID20546718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22616372..22619827hg38UCSC Ensembl
chr10:22905301..22908756hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg383456
hg193456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438065
Supporting Variants
Samples
Known GenesPIP4K2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979678
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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