A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4361738



Internal ID11297590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9970233..9970355hg38UCSC Ensembl
chr19:10080909..10081031hg19UCSC Ensembl
chr19:9941909..9942031hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38123
hg19123
hg18123
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1205344
Supporting Variants
SamplesHuRef
Known GenesCOL5A3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4361738
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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