A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853712



Internal ID22628647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88294789..88316485hg38UCSC Ensembl
chr13:88947044..88968740hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3821697
hg1921697
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853712
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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