A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1329436



Internal ID12145872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14098042..14098110hg38UCSC Ensembl
chr10:14140041..14140109hg19UCSC Ensembl
chr10:14180047..14180115hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3869
hg1969
hg1869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4248639
SamplesHuRef
Known GenesFRMD4A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1329436
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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