A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156867



Internal ID21494275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107901921..107901921hg38UCSC Ensembl
chr7:107542366..107542366hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642762
Supporting Variants
SamplesNA19238
Known GenesDLD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156867
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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