A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1080341



Internal ID11896780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38131818..38131818hg38UCSC Ensembl
chr19:38622458..38622458hg19UCSC Ensembl
chr19:43314298..43314298hg18UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg38975
hg19975
hg18975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3593339
SamplesHuRef
Known GenesSIPA1L3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1080341
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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