A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405857



Internal ID21063410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68755143..68755554hg38UCSC Ensembl
chr5:68050970..68051381hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405857
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