A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118820



Internal ID18935713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:17244991..17246091hg38UCSC Ensembl
Outerchr19:17355800..17356900hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981134
SamplesKWS1
Known GenesNR2F6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118820
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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