A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913810



Internal ID22689026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40136065..40230252hg38UCSC Ensembl
chr7:40175664..40269851hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3894188
hg1994188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445610
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913810
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer