A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441604



Internal ID22499474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77083757..77089390hg38UCSC Ensembl
chr6:77793474..77799107hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg385634
hg195634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441604
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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