A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978699



Internal ID20545739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13904501..13909800hg38UCSC Ensembl
chr10:13946501..13951800hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450120
Supporting Variants
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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