A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845927



Internal ID22620862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65758165..65786305hg38UCSC Ensembl
chr6:66468058..66496198hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3828141
hg1928141
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845927
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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