A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065773



Internal ID21469102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41948736..41948736hg38UCSC Ensembl
chr1:42414407..42414407hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605212
Supporting Variants
SamplesHG03125
Known GenesHIVEP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065773
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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