A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1599327



Internal ID5729430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103822633..103822955hg38UCSC Ensembl
chr7:103463080..103463402hg19UCSC Ensembl
chr7:103250316..103250638hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38323
hg19323
hg18323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3601820
SamplesHuRef
Known GenesRELN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1599327
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer