A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488841



Internal ID21146394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46623842..46642128hg38UCSC Ensembl
chr13:47197977..47216263hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3818287
hg1918287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008536
Samples
Known GenesLRCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488841
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