A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395767



Internal ID21053320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141885501..141888300hg38UCSC Ensembl
chr5:141265066..141267865hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395767
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