A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525723



Internal ID21850081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62818071..62818148hg38UCSC Ensembl
chr2:63045206..63045283hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989743
Supporting Variants
Samples
Known GenesEHBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525723
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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