A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315745



Internal ID20848818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:74748003..74770390hg38UCSC Ensembl
chr1:75213687..75236074hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3822388
hg1922388
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204417
Samples
Known GenesTYW3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315745
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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