A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316072



Internal ID20849149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15776460..15797362hg38UCSC Ensembl
chr1:16102955..16123857hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3820903
hg1920903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200937
Samples
Known GenesFBLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316072
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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