A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867502



Internal ID22642437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34099828..34126582hg38UCSC Ensembl
chr15:34392029..34418783hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3826755
hg1926755
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471238
Samples
Known GenesEMC7, PGBD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867502
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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