A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099128



Internal ID22008361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9221418..9221418hg38UCSC Ensembl
chr12:9374014..9374014hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099128
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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