A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152061



Internal ID21503592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:31334249..31334249hg38UCSC Ensembl
chr7:31373863..31373863hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630548
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152061
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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