A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1027578



Internal ID11844017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14708872..14708937hg38UCSC Ensembl
chr10:14750871..14750936hg19UCSC Ensembl
chr10:14790877..14790942hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3866
hg1966
hg1866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4351205
SamplesHuRef
Known GenesFAM107B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1027578
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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