A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617008



Internal ID20990079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45523445..45523977hg38UCSC Ensembl
chr7:45563044..45563576hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617008
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