A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846004



Internal ID22620939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87429175..87434474hg38UCSC Ensembl
chr6:88138893..88144192hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508471
Samples
Known GenesC6orf165
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846004
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer