A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334600



Internal ID20867787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165031486..165035209hg38UCSC Ensembl
chr1:165000723..165004446hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg383724
hg193724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052809
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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