A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331673



Internal ID20864838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:176844231..176849041hg38UCSC Ensembl
chr1:176813367..176818177hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg384811
hg194811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331673
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