A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393707



Internal ID21051260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44681827..44682386hg38UCSC Ensembl
chr4:44683844..44684403hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117561
Samples
Known GenesGUF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393707
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