A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334860



Internal ID20868049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117403801..117404323hg38UCSC Ensembl
chr1:117946423..117946945hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051846
Samples
Known GenesMAN1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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