A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984931



Internal ID12637058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15604748..15784633hg38UCSC Ensembl
Innerchr9:15604746..15784631hg19UCSC Ensembl
Innerchr9:15594746..15774631hg18UCSC Ensembl
Innerchr9:15594746..15774631hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38179886
hg19179886
hg18179886
hg17179886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752286
Supporting Variants
SamplesSPC_194
Known GenesCCDC171
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984931
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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