A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325979



Internal ID20859113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156198294..156198583hg38UCSC Ensembl
chr1:156168085..156168374hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052255
Samples
Known GenesSLC25A44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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