A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060971



Internal ID21505692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155017347..155017347hg38UCSC Ensembl
chr1:154989823..154989823hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609639
Supporting Variants
SamplesNA19650
Known GenesZBTB7B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060971
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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