A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4012692



Internal ID11749181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31199778..31199778hg38UCSC Ensembl
chr19:31690684..31690684hg19UCSC Ensembl
chr19:36382524..36382524hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38332
hg19332
hg18332
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1467238
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4012692
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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