A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813996



Internal ID21259334
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 StatusM
Merged Variants
Supporting Variantsnssv13704413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813996
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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