A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014046



Internal ID21923389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54565370..54565421hg38UCSC Ensembl
chr7:54633063..54633114hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570443
Samples
Known GenesLOC285878, VSTM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014046
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