A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1481642



Internal ID12298078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15229825..15229924hg38UCSC Ensembl
chr10:15271824..15271923hg19UCSC Ensembl
chr10:15311830..15311929hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38100
hg19100
hg18100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3756316
SamplesHuRef
Known GenesFAM171A1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1481642
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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