A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148623



Internal ID21422758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136045901..136045901hg38UCSC Ensembl
chr6:136367039..136367039hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643709
Supporting Variants
SamplesHG00731
Known GenesPDE7B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148623
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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