A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090830



Internal ID22000063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98490793..98490793hg38UCSC Ensembl
chr12:98884571..98884571hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613587
Samples
Known GenesLOC643770
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090830
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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