A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922260



Internal ID22697485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68058278..68061825hg38UCSC Ensembl
chr10:69818035..69821582hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383548
hg193548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368688
Samples
Known GenesHERC4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922260
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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