A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337247



Internal ID20994800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60648718..60671830hg38UCSC Ensembl
chr2:60875853..60898965hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3823113
hg1923113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337247
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