A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146907



Internal ID21481604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132151456..132151528hg38UCSC Ensembl
chr7:131836215..131836287hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581084
Supporting Variants
SamplesHG03683
Known GenesPLXNA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146907
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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