A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864611



Internal ID22639546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82990908..82992842hg38UCSC Ensembl
chr15:83659660..83661594hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381935
hg191935
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474279, nssv17472347
Samples
Known GenesC15orf40, FAM103A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864611
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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