A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634552



Internal ID21582857
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 StatusM
Merged Variants
Supporting Variantsnssv17155248
SamplesNA18534
Known GenesPTPRZ1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634552
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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