A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904682



Internal ID22679860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35529096..35598351hg38UCSC Ensembl
chr6:35496873..35566128hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3869256
hg1969256
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438122
Samples
Known GenesFKBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904682
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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