A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845598



Internal ID22620533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38761513..38781274hg38UCSC Ensembl
chr6:38729289..38749050hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3819762
hg1919762
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505737
Samples
Known GenesDNAH8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845598
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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