A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157513



Internal ID21512491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140233596..140233596hg38UCSC Ensembl
chr7:139933396..139933396hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632923
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157513
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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