A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914698



Internal ID22689915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35491857..35491906hg38UCSC Ensembl
chr10:35780785..35780834hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368314
Samples
Known GenesCCNY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914698
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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