A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385214



Internal ID22443084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37121963..37129285hg38UCSC Ensembl
chr13:37696100..37703422hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg387323
hg197323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385214
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