A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1399571



Internal ID12216007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:333274..333968hg38UCSC Ensembl
chr19:333274..333968hg19UCSC Ensembl
chr19:284274..284968hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38695
hg19695
hg18695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4160892
SamplesHuRef
Known GenesMIER2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1399571
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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