A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331957



Internal ID20865125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234508863..234510775hg38UCSC Ensembl
chr1:234644609..234646521hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg381913
hg191913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331957
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