A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097306



Internal ID22006539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86469248..86469248hg38UCSC Ensembl
chr10:88229005..88229005hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581488
Samples
Known GenesWAPAL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097306
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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