A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564414



Internal ID22433144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144824437..144824437hg38UCSC Ensembl
chr6:145145573..145145573hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331094, nssv14331093
SamplesHG00731, HG00732
Known GenesUTRN
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564414
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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