A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990045



Internal ID12637040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15578019..15794899hg38UCSC Ensembl
Innerchr9:15578017..15794897hg19UCSC Ensembl
Innerchr9:15568017..15784897hg18UCSC Ensembl
Innerchr9:15568017..15784897hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38216881
hg19216881
hg18216881
hg17216881
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)essv6990045
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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