A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132596



Internal ID19253795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:190093545..190119845hg38UCSC Ensembl
Outerchr4:191014700..191041000hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3826301
hg1926301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3007n106
Supporting Variantsnssv3987382
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132596
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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