A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861735



Internal ID22636670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24623494..24690893hg38UCSC Ensembl
chr13:25197632..25265031hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3867400
hg1967400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463436
Samples
Known GenesATP12A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861735
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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