A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14356801



Internal ID22186048
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208949
Supporting Variants
SamplesHG00731
Known GenesNUDC
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14356801
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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