A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065235



Internal ID21511532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40059014..40059014hg38UCSC Ensembl
chr1:40524686..40524686hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607027
Supporting Variants
SamplesNA24385
Known GenesCAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065235
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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