A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871031



Internal ID22645969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21324324..21354141hg38UCSC Ensembl
chr17:21227636..21257453hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3829818
hg1929818
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472448, nssv17476231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871031
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