A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845090



Internal ID22620025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2187120..2197117hg38UCSC Ensembl
chr6:2187354..2197351hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg389998
hg199998
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503783
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845090
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