A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913761



Internal ID22688977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121673768..121701904hg38UCSC Ensembl
chr10:123433282..123461418hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3828137
hg1928137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913761
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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