A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844667



Internal ID22619602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151982415..151990622hg38UCSC Ensembl
chr6:152303550..152311757hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg388208
hg198208
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501659
Samples
Known GenesESR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844667
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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