A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414425



Internal ID22472295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14739241..14740740hg38UCSC Ensembl
chr6:14739472..14740971hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906112
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414425
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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