A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978745



Internal ID20545785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14934614..15017118hg38UCSC Ensembl
chr10:14976613..15059117hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3882505
hg1982505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446306
Supporting Variants
Samples
Known GenesDCLRE1C, MEIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978745
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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