A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135927



Internal ID18902168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:48365363..48365441hg38UCSC Ensembl
Outerchr19:48868620..48868698hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1793n106
Supporting Variantsnssv3989524
SamplesKWS1
Known GenesSYNGR4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135927
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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