A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856485



Internal ID22631420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68057927..68061307hg38UCSC Ensembl
chr10:69817684..69821064hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383381
hg193381
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453400
Samples
Known GenesHERC4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856485
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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