A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1123063



Internal ID11939500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59882097..59882341hg38UCSC Ensembl
chr10:61641855..61642099hg19UCSC Ensembl
chr10:61311861..61312105hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38245
hg19245
hg18245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4081767
SamplesHuRef
Known GenesCCDC6
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1123063
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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