A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073441



Internal ID19323889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16179190..16179991hg38UCSC Ensembl
chr5:16179299..16180100hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770487
SamplesKWP1
Known GenesMARCH11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073441
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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