A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681785



Internal ID21203645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11330941..11330941hg38UCSC Ensembl
chr2:11471067..11471067hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2805304
Supporting Variants
Samples
Known GenesROCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681785
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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