A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872033



Internal ID22646971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39023377..39030780hg38UCSC Ensembl
chr17:37179630..37187033hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387404
hg197404
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478230
Samples
Known GenesLRRC37A11P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872033
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