A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148822



Internal ID21468214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165339906..165339956hg38UCSC Ensembl
chr6:165753395..165753445hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571160
Supporting Variants
SamplesHG03125
Known GenesPDE10A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148822
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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