A curated catalogue of human genomic structural variation




Variant Details

Variant: esv991439



Internal ID6727403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75352103..75352103hg38UCSC Ensembl
chr10:77111861..77111861hg19UCSC Ensembl
chr10:76781867..76781867hg18UCSC 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 Variantsessv3583295
SamplesHuRef
Known GenesZNF503-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv991439
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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