A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152270



Internal ID21505831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41173689..41173689hg38UCSC Ensembl
chr7:41213287..41213287hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644067
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152270
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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