A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640906



Internal ID21832953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8411648..8411648hg38UCSC Ensembl
chrUn_gl000220:127253..127253hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640906
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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