A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377577



Internal ID22435447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38954081..38955889hg38UCSC Ensembl
chr13:39528218..39530026hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381809
hg191809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377577
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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