A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912779



Internal ID22687995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73799896..73800197hg38UCSC Ensembl
chr7:73214226..73214527hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912779
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