A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3612695



Internal ID12149173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15616132..15616132hg38UCSC Ensembl
chr19:15726943..15726943hg19UCSC Ensembl
chr19:15587943..15587943hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3897
hg1997
hg1897
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1497518
Supporting Variants
SamplesHuRef
Known GenesCYP4F8
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3612695
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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