A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119044



Internal ID19273741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:149649437..149650137hg38UCSC Ensembl
Outerchr5:149029000..149029700hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981841
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119044
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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