A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147411



Internal ID346592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108025435..108025437hg38UCSC Ensembl
chr7:107665880..107665882hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg383
hg193
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004080
Samples
Known GenesLAMB4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147411
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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