A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852985



Internal ID22627920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51965483..51968093hg38UCSC Ensembl
chr13:52539619..52542229hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg382611
hg192611
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469293
Samples
Known GenesATP7B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852985
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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