A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148084



Internal ID21508418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2504580..2504580hg38UCSC Ensembl
chr6:2504814..2504814hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630841
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148084
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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