A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980653



Internal ID20547693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13057445..13067528hg38UCSC Ensembl
chr10:13099445..13109528hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3810084
hg1910084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441273
Supporting Variants
Samples
Known GenesCCDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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