A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012797



Internal ID21922140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160653249..160653348hg38UCSC Ensembl
chr5:160080256..160080355hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574646
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012797
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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