A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396181



Internal ID21053734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53856831..53857269hg38UCSC Ensembl
chr6:53721629..53722067hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144693
Samples
Known GenesLRRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396181
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