A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980107



Internal ID12634573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485135..69519460hg38UCSC Ensembl
Innerchr9:72100051..72134376hg19UCSC Ensembl
Innerchr9:71289871..71324196hg18UCSC Ensembl
Innerchr9:69329605..69363930hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3834326
hg1934326
hg1834326
hg1734326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34446
Supporting Variants
SamplesNA18953
Known GenesAPBA1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980107
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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