A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13676778



Internal ID21198631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24344991..24344991hg38UCSC Ensembl
chr1:24671481..24671481hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801458
Supporting Variants
Samples
Known GenesGRHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13676778
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.555556


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