A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871612



Internal ID22646550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97537115..97599377hg38UCSC Ensembl
chr15:98080345..98142607hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3862263
hg1962263
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474992
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871612
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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