A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1455501



Internal ID5585608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39015585..39015640hg38UCSC Ensembl
chr7:39055185..39055240hg19UCSC Ensembl
chr7:39021710..39021765hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3877351
SamplesHuRef
Known GenesPOU6F2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1455501
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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