A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319760



Internal ID20852856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101493070..101508760hg38UCSC Ensembl
chr1:101958626..101974316hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3815691
hg1915691
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319760
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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