A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632922



Internal ID21581227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132151336..132151336hg38UCSC Ensembl
chr7:131836095..131836095hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146440
SamplesNA24385
Known GenesPLXNA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632922
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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