A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603797



Internal ID20976868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165394801..165396900hg38UCSC Ensembl
chr6:165808290..165810389hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142396
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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