A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607178



Internal ID20980249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150754414..150757048hg38UCSC Ensembl
chr6:151075550..151078184hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382635
hg192635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141047
Samples
Known GenesPLEKHG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607178
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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