A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385736



Internal ID21043289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71294814..71304563hg38UCSC Ensembl
chr4:72160531..72170280hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg389750
hg199750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211734
Samples
Known GenesSLC4A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385736
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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