A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319235



Internal ID20852327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14145551..14149254hg38UCSC Ensembl
chr1:14472046..14475749hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg383704
hg193704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319235
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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