A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350767



Internal ID21008320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235076433..235076703hg38UCSC Ensembl
chr2:235985077..235985347hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350767
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