A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607460



Internal ID20980531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150602101..150620618hg38UCSC Ensembl
chr6:150923237..150941754hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3818518
hg1918518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141038
Samples
Known GenesPLEKHG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607460
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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