A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1218372



Internal ID12381495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21258603..21258777hg38UCSC Ensembl
chr10:21547532..21547706hg19UCSC Ensembl
chr10:21587538..21587712hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38175
hg19175
hg18175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4044289
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1218372
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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