A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985863



Internal ID20552903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99340257..99341705hg38UCSC Ensembl
chr10:101100014..101101462hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381449
hg191449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443287
Supporting Variants
Samples
Known GenesCNNM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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