A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065191



Internal ID21504903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37239699..37239699hg38UCSC Ensembl
chr1:37705300..37705300hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618711
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065191
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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