A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067243



Internal ID21976476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1890521..1890521hg38UCSC Ensembl
chr6:1890755..1890755hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562252
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067243
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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