A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111047



Internal ID21505988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207095684..207095684hg38UCSC Ensembl
chr2:207960408..207960408hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606264
Supporting Variants
SamplesNA19983
Known GenesKLF7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111047
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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