A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892178



Internal ID22667224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89052053..89055372hg38UCSC Ensembl
chr6:89761772..89765091hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383320
hg193320
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1791n209
Supporting Variantsnssv17440616, nssv17436865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892178
Frequency
Sample Size914
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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