A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3931034



Internal ID11484152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8054990..8055472hg38UCSC Ensembl
chr19:8119874..8120356hg19UCSC Ensembl
chr19:8025874..8026356hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38483
hg19483
hg18483
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1497112
Supporting Variants
SamplesHuRef
Known GenesCCL25
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3931034
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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