A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852509



Internal ID22627444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155179716..155188348hg38UCSC Ensembl
chr7:154971426..154980058hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg388633
hg198633
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852509
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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