A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865945



Internal ID22640880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78002036..78003742hg38UCSC Ensembl
chr13:78576171..78577877hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg381707
hg191707
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453483, nssv17456747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865945
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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