A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846736



Internal ID22621671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53701250..53709819hg38UCSC Ensembl
chr7:53768943..53777512hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg388570
hg198570
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507772
Samples
Known GenesFLJ45974
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846736
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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