A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857201



Internal ID22632136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44530005..44532204hg38UCSC Ensembl
chr15:44822203..44824402hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471645, nssv17471646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857201
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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