A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846853



Internal ID22621788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38872424..38895867hg38UCSC Ensembl
chr7:38912024..38935467hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3823444
hg1923444
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506401
Samples
Known GenesVPS41
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846853
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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