A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334328



Internal ID20867512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113023984..113029319hg38UCSC Ensembl
chr1:113566606..113571941hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg385336
hg195336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051364
Samples
Known GenesLOC100996251
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334328
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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