A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334660



Internal ID20867847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174997101..175003500hg38UCSC Ensembl
chr1:174966238..174972636hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg386400
hg196399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201053
Samples
Known GenesCACYBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334660
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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