A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1159408



Internal ID11975846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29010206..29010206hg38UCSC Ensembl
chr19:29501113..29501113hg19UCSC Ensembl
chr19:34192953..34192953hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38158
hg19158
hg18158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4042003
SamplesHuRef
Known GenesLOC100505835
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1159408
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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