A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1292577



Internal ID12109013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14568418..14568418hg38UCSC Ensembl
chr10:14610417..14610417hg19UCSC Ensembl
chr10:14650423..14650423hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38321
hg19321
hg18321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4134415
SamplesHuRef
Known GenesFAM107B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1292577
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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