A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471769



Internal ID22529661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70877735..70883785hg38UCSC Ensembl
chr15:71170074..71176124hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386051
hg196051
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848507
Supporting Variants
Samples
Known GenesLRRC49, THAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471769
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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