A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410648



Internal ID22468518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13882318..13883620hg38UCSC Ensembl
chr6:13882549..13883851hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381303
hg191303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894571
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410648
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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