A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320107



Internal ID20853205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31051462..31056881hg38UCSC Ensembl
chr1:31524309..31529728hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg385420
hg195420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060359
Samples
Known GenesPUM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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