A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752287



Internal ID12639153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17593260..17632545hg38UCSC Ensembl
Innerchr9:17593258..17632543hg19UCSC Ensembl
Innerchr9:17583258..17622543hg18UCSC Ensembl
Innerchr9:17583258..17622543hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3839286
hg1939286
hg1839286
hg1739286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6985926, essv6985927
SamplesSPC_85
Known GenesSH3GL2
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)esv2752287
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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