A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15203983



Internal ID21342789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132151336..132151336hg38UCSC Ensembl
chr7:131836095..131836095hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3933256
Supporting Variants
SamplesHG002
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15203983
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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