A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1167286



Internal ID11983723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3406336..3406470hg38UCSC Ensembl
chr19:3406334..3406468hg19UCSC Ensembl
chr19:3357334..3357468hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38135
hg19135
hg18135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4024912
SamplesHuRef
Known GenesNFIC
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1167286
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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