A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752153



Internal ID12985705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19469379..19581028hg38UCSC Ensembl
Innerchr7:19509002..19620651hg19UCSC Ensembl
Innerchr7:19475527..19587176hg18UCSC Ensembl
Innerchr7:19282242..19393891hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38111650
hg19111650
hg18111650
hg17111650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6990129, essv6985715, essv6990128, essv6985714
SamplesSPC_36
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)esv2752153
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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