A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752286



Internal ID12639152
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 StatusM
Merged Variants
Supporting Variantsessv6984930, essv6984931, essv6990045
SamplesSPC_194
Known GenesCCDC171
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)esv2752286
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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