A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438122



Internal ID22495992
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 StatusS
Merged Variantsnsv5904682
Supporting Variants
Samples
Known GenesFKBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438122
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003


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