A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551909



Internal ID20925041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57602973..58277049hg38UCSC Ensembl
chr3:57588700..58262776hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38674077
hg19674077
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261535
Samples
Known GenesABHD6, DENND6A, DNASE1L3, FLNB, SLMAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551909
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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