A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897995



Internal ID22673106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121814743..121832105hg38UCSC Ensembl
chr6:122135889..122153251hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3817363
hg1917363
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897995
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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