A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377029



Internal ID21034582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:72948827..73184927hg38UCSC Ensembl
chr4:73814544..74050644hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38236101
hg19236101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212343
Samples
Known GenesANKRD17, COX18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377029
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