A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3779588



Internal ID11635597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71760149..71760223hg38UCSC Ensembl
chr10:73519906..73519980hg19UCSC Ensembl
chr10:73189912..73189986hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3875
hg1975
hg1875
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1096295
Supporting Variants
SamplesHuRef
Known GenesC10orf54, CDH23, MIR6797
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3779588
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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