A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613724



Internal ID20986795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21281203..21281478hg38UCSC Ensembl
chr7:21320821..21321096hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156947
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613724
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