A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064070



Internal ID21469376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:245264936..245264936hg38UCSC Ensembl
chr1:245428238..245428238hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612943
Supporting Variants
SamplesHG03125
Known GenesKIF26B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064070
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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