A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070549



Internal ID21979782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36681521..36681521hg38UCSC Ensembl
chr6:36649298..36649298hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559383
Samples
Known GenesCDKN1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070549
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer