A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925810



Internal ID22701037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91439526..91455986hg38UCSC Ensembl
chr10:93199283..93215743hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3816461
hg1916461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365498
Samples
Known GenesHECTD2, LOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925810
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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