A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064645



Internal ID21433894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25529499..25529499hg38UCSC Ensembl
chr1:25855990..25855990hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620195
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064645
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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