A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1495837



Internal ID12312274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11874571..11874571hg38UCSC Ensembl
chr18:11874570..11874570hg19UCSC Ensembl
chr18:11864570..11864570hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38456
hg19456
hg18456
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3858426
SamplesHuRef
Known GenesGNAL
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1495837
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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