A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845730



Internal ID22620665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81967387..81969837hg38UCSC Ensembl
chr6:82677104..82679554hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382451
hg192451
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845730
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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