A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380645



Internal ID21038198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56099941..56242882hg38UCSC Ensembl
chr4:56966107..57109048hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38142942
hg19142942
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211951
Samples
Known GenesKIAA1211
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380645
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