A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703918



Internal ID21225726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170126072..170126072hg38UCSC Ensembl
chr6:170441296..170441296hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813645
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703918
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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