A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315702



Internal ID20848774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159150301..159153300hg38UCSC Ensembl
chr1:159120091..159123090hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053499
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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