A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149647



Internal ID21509923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44202428..44202428hg38UCSC Ensembl
chr6:44170165..44170165hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382915
hg192915
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639028
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149647
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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