A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845957



Internal ID22620892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73382869..73390031hg38UCSC Ensembl
chr6:74092592..74099754hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg387163
hg197163
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845957
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