A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323738



Internal ID20856859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13783959..13785179hg38UCSC Ensembl
chr1:14110454..14111674hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051526
Samples
Known GenesPRDM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323738
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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