A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689075



Internal ID21210927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97571601..97571601hg38UCSC Ensembl
chr13:98223855..98223855hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689075
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.5625


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