A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706771



Internal ID21228564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173964515..173964579hg38UCSC Ensembl
chr5:173391518..173391582hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2812218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706771
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.5


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