A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3922943



Internal ID11838928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69286017..69286017hg38UCSC Ensembl
chr15:69578356..69578356hg19UCSC Ensembl
chr15:67365410..67365410hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3871
hg1971
hg1871
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1316872
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3922943
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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