A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123670



Internal ID21496996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35772679..35772679hg38UCSC Ensembl
chr4:35774301..35774301hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605422
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123670
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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