A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985734



Internal ID20552774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95268862..95271632hg38UCSC Ensembl
chr10:97028619..97031389hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382771
hg192771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451399
Supporting Variants
Samples
Known GenesPDLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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