A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850782



Internal ID22625717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62010320..62074896hg38UCSC Ensembl
chr15:62302519..62367095hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3864577
hg1964577
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472972
Samples
Known GenesC2CD4A, VPS13C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850782
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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