A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149617



Internal ID21454298
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 Variantsnsv5583813
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149617
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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