A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436436



Internal ID22494306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116424599..116424673hg38UCSC Ensembl
chr7:116064653..116064727hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911376
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436436
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