A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707413



Internal ID21229185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163574158..163574222hg38UCSC Ensembl
chr5:163001164..163001228hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810577
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707413
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.551724


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