A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855663



Internal ID22630598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137262797..137268459hg38UCSC Ensembl
chr7:136947544..136953206hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg385663
hg195663
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501344
Samples
Known GenesPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855663
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