A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845121



Internal ID22620056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29656780..29657811hg38UCSC Ensembl
chr6:29624557..29625588hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381032
hg191032
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504446
Samples
Known GenesMOG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845121
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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