A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559590



Internal ID21883945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149682491..149682560hg38UCSC Ensembl
chr6:150003627..150003696hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015603
Supporting Variants
Samples
Known GenesLATS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559590
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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