A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614651



Internal ID20987722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150036665..150088330hg38UCSC Ensembl
chr6:150357801..150409466hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3851666
hg1951666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140999
Samples
Known GenesULBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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