A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382005



Internal ID21039558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:179729231..182727604hg38UCSC Ensembl
chr4:180650384..183648757hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg382998374
hg192998374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115073
Samples
Known GenesLINC00290, MGC45800, MIR1305, TENM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382005
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