A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315930



Internal ID20849005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94253864..94263878hg38UCSC Ensembl
chr1:94719420..94729434hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3810015
hg1910015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315930
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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