A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1653674



Internal ID12816792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:810297..810297hg38UCSC Ensembl
chr17:713537..713537hg19UCSC Ensembl
chr17:660287..660287hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38508
hg19508
hg18508
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3589749
SamplesHuRef
Known GenesNXN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1653674
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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