A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1497662



Internal ID12660784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4191461..4192108hg38UCSC Ensembl
chr17:4094756..4095403hg19UCSC Ensembl
chr17:4041505..4042152hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38648
hg19648
hg18648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4020247
SamplesHuRef
Known GenesANKFY1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1497662
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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