A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064286



Internal ID21433754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25724513..25724513hg38UCSC Ensembl
chr1:26051004..26051004hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604585
Supporting Variants
SamplesHG00731
Known GenesMAN1C1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064286
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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