A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1076637



Internal ID11893076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45084217..45084337hg38UCSC Ensembl
chr7:45123816..45123936hg19UCSC Ensembl
chr7:45090341..45090461hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38121
hg19121
hg18121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3611828
SamplesHuRef
Known GenesNACAD
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1076637
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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