A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845358



Internal ID22620293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71159202..71165324hg38UCSC Ensembl
chr6:71868905..71875027hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg386123
hg196123
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845358
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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