A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13680872



Internal ID21202731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11618129..11618129hg38UCSC Ensembl
chr2:11758255..11758255hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804974
Supporting Variants
Samples
Known GenesGREB1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13680872
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.370968


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