A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870915



Internal ID22645852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85277326..85277473hg38UCSC Ensembl
chr1:85743009..85743156hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372751
Samples
Known GenesLOC646626
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870915
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer