A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603995



Internal ID20977066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165566313..165566959hg38UCSC Ensembl
chr6:165979801..165980447hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142411
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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