A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075937



Internal ID21985170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61658855..61658855hg38UCSC Ensembl
chr8:62571414..62571414hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585518
Samples
Known GenesASPH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075937
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