A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456195



Internal ID22514072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114270251..114272912hg38UCSC Ensembl
chr13:115035726..115038387hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382662
hg192662
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850102
Supporting Variants
Samples
Known GenesCDC16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456195
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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