A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319820



Internal ID20852917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166945801..166950500hg38UCSC Ensembl
chr1:166915038..166919737hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201963
Samples
Known GenesILDR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319820
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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