A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328337



Internal ID20861484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207020925..207021298hg38UCSC Ensembl
chr1:207194270..207194643hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057114
Samples
Known GenesC1orf116
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328337
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