A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335371



Internal ID20868563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175299241..175338809hg38UCSC Ensembl
chr1:175268377..175307945hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3839569
hg1939569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201068
Samples
Known GenesTNR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335371
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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