A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017555



Internal ID21926898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44044442..44045418hg38UCSC Ensembl
chr6:44012179..44013155hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017555
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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