A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043524



Internal ID21952818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58698102..58698102hg38UCSC Ensembl
chr1:59163774..59163774hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527159
Samples
Known GenesMYSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043524
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