A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860401



Internal ID22635336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77705213..77710220hg38UCSC Ensembl
chr13:78279348..78284355hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg385008
hg195008
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463363
Samples
Known GenesSLAIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860401
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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