A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844886



Internal ID22619821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37504559..37531879hg38UCSC Ensembl
chr6:37472335..37499655hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3827321
hg1927321
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844886
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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