A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319240



Internal ID20852332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94713470..94713593hg38UCSC Ensembl
chr1:95179026..95179149hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065652
Samples
Known GenesLINC01057
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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