A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862637



Internal ID22637572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132281352..132283385hg38UCSC Ensembl
chr7:131966111..131968144hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg382034
hg192034
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503944, nssv17501278
Samples
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862637
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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