A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404165



Internal ID21061718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82918786..82919404hg38UCSC Ensembl
chr5:82214605..82215223hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133014
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404165
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