A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763584



Internal ID18963508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145482047..145482448hg38UCSC Ensembl
chr4:146403199..146403600hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074222
Supporting Variants
SamplesKWP1
Known GenesSMAD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763584
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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