A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3569155



Internal ID6693851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72928052..72928052hg38UCSC Ensembl
chr9:75542968..75542968hg19UCSC Ensembl
chr9:74732788..74732788hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38349
hg19349
hg18349
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991190
Supporting Variants
SamplesHuRef
Known GenesALDH1A1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3569155
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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