A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751157



Internal ID12638023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98089059..98147329hg38UCSC Ensembl
Innerchr13:98741313..98799583hg19UCSC Ensembl
Innerchr13:97539314..97597584hg18UCSC Ensembl
Innerchr13:97539314..97597584hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3858271
hg1958271
hg1858271
hg1758271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6989821, essv6983585
SamplesBEC_670
Known GenesFARP1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751157
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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