A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326151



Internal ID20859285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17444817..17521470hg38UCSC Ensembl
chr1:17771313..17847966hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3876654
hg1976654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326151
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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