A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1490079



Internal ID12306515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75352141..75352141hg38UCSC Ensembl
chr10:77111899..77111899hg19UCSC Ensembl
chr10:76781905..76781905hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38229
hg19229
hg18229
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4090692
SamplesHuRef
Known GenesZNF503-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1490079
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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