A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320213



Internal ID20853311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15785468..15790332hg38UCSC Ensembl
chr1:16111963..16116827hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384865
hg194865
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200939
Samples
Known GenesFBLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320213
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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