A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333832



Internal ID20867013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150940353..150940833hg38UCSC Ensembl
chr1:150912829..150913309hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053005
Samples
Known GenesSETDB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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