A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060848



Internal ID21506192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156004399..156004399hg38UCSC Ensembl
chr1:155974190..155974190hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620501
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060848
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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