A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845514



Internal ID22620449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43006921..43029742hg38UCSC Ensembl
chr6:42974659..42997480hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3822822
hg1922822
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505794
Samples
Known GenesKLHDC3, MEA1, PPP2R5D, RRP36
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845514
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