A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395257



Internal ID21052810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140285359..140301816hg38UCSC Ensembl
chr4:141206513..141222970hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3816458
hg1916458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108098
Samples
Known GenesLOC100129858, SCOC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395257
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