A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073323



Internal ID19318227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43286082..43289883hg38UCSC Ensembl
chr4:43288099..43291900hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg383802
hg193802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3761993
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073323
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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