A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327449



Internal ID20860588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157874638..157878746hg38UCSC Ensembl
chr1:157844428..157848536hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg384109
hg194109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327449
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