A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335217



Internal ID20868409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202406206..202412014hg38UCSC Ensembl
chr1:202375334..202381142hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg385809
hg195809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056684
Samples
Known GenesPPP1R12B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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