A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315868



Internal ID20848942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44111872..44115429hg38UCSC Ensembl
chr1:44577544..44581101hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg383558
hg193558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061376
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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