A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1069815



Internal ID5199922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42338240..42338460hg38UCSC Ensembl
chr17:40490258..40490478hg19UCSC Ensembl
chr17:37743784..37744004hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38221
hg19221
hg18221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3767990
SamplesHuRef
Known GenesSTAT3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1069815
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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