A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698537



Internal ID21220388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44710978..44710978hg38UCSC Ensembl
chr6:44678715..44678715hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698537
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.5


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