A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317279



Internal ID20850363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3004990..3396785hg38UCSC Ensembl
chr1:2921554..3313349hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38391796
hg19391796
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203562
Samples
Known GenesACTRT2, LINC00982, MIR4251, PRDM16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317279
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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