A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347135



Internal ID21004688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180141344..180141970hg38UCSC Ensembl
chr2:181006071..181006697hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347135
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