A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2812002



Internal ID21257340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168755390..168755390hg38UCSC Ensembl
chr5:168182395..168182395hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13704811
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2812002
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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