A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907629



Internal ID22682839
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 StatusM
Merged Variants
Supporting Variantsnssv17364859
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907629
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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