A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328069



Internal ID20861214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26171277..26189545hg38UCSC Ensembl
chr1:26497768..26516036hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3818269
hg1918269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203466
Samples
Known GenesCNKSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328069
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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