A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380844



Internal ID21038397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38285374..38285913hg38UCSC Ensembl
chr5:38285476..38286015hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130725
Samples
Known GenesEGFLAM, EGFLAM-AS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380844
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