A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010496



Internal ID7059838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29457290..29465260hg38UCSC Ensembl
Outerchr19:29948197..29956167hg19UCSC Ensembl
Outerchr19:34640037..34648007hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg387971
hg197971
hg187971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564307
SamplesHuRef
Known GenesLOC284395
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010496
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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