A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700056



Internal ID21221892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66431846..66431846hg38UCSC Ensembl
chr2:66658978..66658978hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806552
Supporting Variants
Samples
Known GenesMEIS1-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700056
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.5


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