A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141109



Internal ID21496793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5930763..5930763hg38UCSC Ensembl
chr7:5970394..5970394hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643191
Supporting Variants
SamplesNA19238
Known GenesRSPH10B, RSPH10B2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141109
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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