A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146550



Internal ID21456960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146161427..146161427hg38UCSC Ensembl
chr7:145858519..145858519hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639803
Supporting Variants
SamplesHG02587
Known GenesCNTNAP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146550
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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