A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536960



Internal ID21861315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9907967..9907967hg38UCSC Ensembl
chr1:9968025..9968025hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042163
Supporting Variants
Samples
Known GenesCTNNBIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536960
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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