A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433543



Internal ID21091096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155084842..155088916hg38UCSC Ensembl
chr7:154876552..154880626hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg384075
hg194075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219745
Samples
Known GenesHTR5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433543
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