A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319067



Internal ID20852159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:116670529..116680528hg38UCSC Ensembl
chr1:117213151..117223150hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199752
Samples
Known GenesMIR320B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319067
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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