A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158458



Internal ID21494033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120314004..120314004hg38UCSC Ensembl
chr7:119954058..119954058hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637680
Supporting Variants
SamplesNA19238
Known GenesKCND2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158458
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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