A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527801



Internal ID22397188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109729224..109729306hg38UCSC Ensembl
chr13:110381571..110381653hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14368647, nssv14368646
SamplesHG00731, HG00733
Known GenesLINC00676
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527801
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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