A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073851



Internal ID19324814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4842846..4843382hg38UCSC Ensembl
chr5:4842959..4843495hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764931
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073851
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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