A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364859



Internal ID22590528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18914455..19049658hg38UCSC Ensembl
chr10:19203384..19338587hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38135204
hg19135204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907629
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364859
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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