A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334227



Internal ID20867410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202519940..202549398hg38UCSC Ensembl
chr1:202489068..202518526hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3829459
hg1929459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056689
Samples
Known GenesPPP1R12B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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