A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1683190



Internal ID12846308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15960273..15960591hg38UCSC Ensembl
chr17:15863587..15863905hg19UCSC Ensembl
chr17:15804312..15804630hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38319
hg19319
hg18319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4183907
SamplesHuRef
Known GenesADORA2B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1683190
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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