A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333486



Internal ID20866663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1650928..1717340hg38UCSC Ensembl
chr1:1584547..1648779hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3866413
hg1964233
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv25n223
Supporting Variantsnssv18201929
Samples
Known GenesCDK11A, CDK11B, MMP23A, SLC35E2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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