A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208949



Internal ID22357099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26931455..26931735hg38UCSC Ensembl
chr1:27257946..27258226hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14356801, nssv14356800
SamplesHG00731, HG00513
Known GenesNUDC
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208949
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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