A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325231



Internal ID20858362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155076639..155108603hg38UCSC Ensembl
chr1:155049115..155081079hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3831965
hg1931965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200511
Samples
Known GenesEFNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325231
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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