A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4036019



Internal ID11379169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11402999..11403531hg38UCSC Ensembl
chr19:11513675..11514207hg19UCSC Ensembl
chr19:11374675..11375207hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38533
hg19533
hg18533
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1464086
Supporting Variants
SamplesHuRef
Known GenesRGL3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4036019
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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