A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325508



Internal ID20858639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13985052..14044906hg38UCSC Ensembl
chr1:14311547..14371401hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3859855
hg1959855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325508
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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