A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619636



Internal ID20992707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20282427..20282803hg38UCSC Ensembl
chr7:20322050..20322426hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619636
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