A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509836



Internal ID20883148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45580001..45630600hg38UCSC Ensembl
chr17:43657367..43707966hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3850600
hg1950600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3125n223
Supporting Variantsnssv18180137
Samples
Known GenesCRHR1, LOC644172, MGC57346
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509836
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