A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537189



Internal ID21861544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66431845..66431845hg38UCSC Ensembl
chr2:66658977..66658977hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043472
Supporting Variants
Samples
Known GenesMEIS1-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537189
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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