A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1398603



Internal ID12561725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58074277..58074454hg38UCSC Ensembl
chr17:56151638..56151815hg19UCSC Ensembl
chr17:53506637..53506814hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38178
hg19178
hg18178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3588437
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1398603
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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