A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685872



Internal ID21207729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:60281289..60281289hg38UCSC Ensembl
chr12:60675070..60675070hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791682
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685872
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.078125


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