A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704413



Internal ID21226218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167997485..167997485hg38UCSC Ensembl
chr6:168398165..168398165hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813996
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704413
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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