A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1366836



Internal ID12183273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37021645..37021839hg38UCSC Ensembl
chr17:35378944..35379138hg19UCSC Ensembl
chr17:32453057..32453251hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38195
hg19195
hg18195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3980266
SamplesHuRef
Known GenesAATF
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1366836
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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