A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848507



Internal ID22623442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70877735..70883785hg38UCSC Ensembl
chr15:71170074..71176124hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386051
hg196051
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471769
Samples
Known GenesLRRC49, THAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848507
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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