A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331837



Internal ID20865004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151262750..151263379hg38UCSC Ensembl
chr1:151235226..151235855hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051319
Samples
Known GenesPSMD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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