A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074798



Internal ID18975498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1273714..1273790hg38UCSC Ensembl
chr5:1273829..1273905hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768148
SamplesKWP1
Known GenesTERT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074798
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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