A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133449



Internal ID18910094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35268197..35269497hg38UCSC Ensembl
Outerchr19:35759100..35760400hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989900, nssv3981141
SamplesKWS1, KWS2
Known GenesUSF2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133449
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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