A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402883



Internal ID21060436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73324000..73364974hg38UCSC Ensembl
chr6:74033723..74074697hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3840975
hg1940975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229096
Samples
Known GenesDPPA5, KHDC3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402883
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