A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148384



Internal ID21468072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135641681..135641681hg38UCSC Ensembl
chr7:135326429..135326429hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628825
Supporting Variants
SamplesHG03125
Known GenesNUP205
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148384
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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