A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081862



Internal ID21991095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29410831..29410831hg38UCSC Ensembl
chr10:29699760..29699760hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588230
Samples
Known GenesPTCHD3P1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081862
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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