A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1648968



Internal ID5779069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71496825..71496945hg38UCSC Ensembl
chr10:73256582..73256702hg19UCSC Ensembl
chr10:72926588..72926708hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38121
hg19121
hg18121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4268365
SamplesHuRef
Known GenesCDH23
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1648968
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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