A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064075



Internal ID20631115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75969963..75970337hg38UCSC Ensembl
chr1:76435648..76436022hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326272
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00113


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