A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073883



Internal ID19323430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55896471..55897272hg38UCSC Ensembl
chr5:55192299..55193100hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769045
SamplesKWP1
Known GenesIL31RA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073883
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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