A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571976



Internal ID21764019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92513339..92513402hg38UCSC Ensembl
chr7:92142653..92142716hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011054
Supporting Variants
Samples
Known GenesPEX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571976
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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