A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344581



Internal ID21002134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237161700..237162538hg38UCSC Ensembl
chr2:238070343..238071181hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38839
hg19839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344581
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