A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845733



Internal ID22620668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84046959..84054480hg38UCSC Ensembl
chr6:84756678..84764199hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg387522
hg197522
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503131
Samples
Known GenesMRAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845733
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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