A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1406871



Internal ID12223307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67731255..67731531hg38UCSC Ensembl
chr17:65727371..65727647hg19UCSC Ensembl
chr17:63157833..63158109hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38277
hg19277
hg18277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4144741
SamplesHuRef
Known GenesNOL11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1406871
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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