A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377186



Internal ID21034739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:124675294..124676037hg38UCSC Ensembl
chr4:125596449..125597192hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109823
Samples
Known GenesANKRD50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377186
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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