A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074878



Internal ID18977777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150366538..150366958hg38UCSC Ensembl
chr5:149746101..149746521hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771421
SamplesKWP1
Known GenesTCOF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074878
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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