A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4081767



Internal ID11333422
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1123063
Supporting Variants
SamplesHuRef
Known GenesCCDC6
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4081767
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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