A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637680



Internal ID21585985
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 StatusM
Merged Variants
Supporting Variantsnssv17158458
SamplesNA19238
Known GenesKCND2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637680
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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