A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155248



Internal ID21488080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121935493..121935493hg38UCSC Ensembl
chr7:121575547..121575547hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634552
Supporting Variants
SamplesNA18534
Known GenesPTPRZ1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155248
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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