A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752281



Internal ID12639147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13284601..13405073hg38UCSC Ensembl
Innerchr9:13284600..13405072hg19UCSC Ensembl
Innerchr9:13274600..13395072hg18UCSC Ensembl
Innerchr9:13274600..13395072hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38120473
hg19120473
hg18120473
hg17120473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6985737, essv6989497, essv6985736, essv6990134
SamplesSPC_38
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752281
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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