A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340342



Internal ID20997895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:30605952..30609326hg38UCSC Ensembl
chr2:30828818..30832192hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg383375
hg193375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085201
Samples
Known GenesLCLAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340342
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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