A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600543



Internal ID20973614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150621473..150629468hg38UCSC Ensembl
chr6:150942609..150950604hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg387996
hg197996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141040
Samples
Known GenesPLEKHG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600543
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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