A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528880



Internal ID21853237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31353758..31353758hg38UCSC Ensembl
chr2:31576624..31576624hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6055264
Supporting Variants
Samples
Known GenesXDH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528880
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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