A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861607



Internal ID22636542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82993293..83003408hg38UCSC Ensembl
chr15:83662045..83672160hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3810116
hg1910116
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474280
Samples
Known GenesC15orf40
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861607
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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