A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349204



Internal ID21006757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186027430..186069360hg38UCSC Ensembl
chr2:186892157..186934087hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3841931
hg1941931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349204
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