A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536301



Internal ID21860656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64544650..64544650hg38UCSC Ensembl
chr2:64771784..64771784hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042875
Supporting Variants
Samples
Known GenesAFTPH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536301
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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