A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752015



Internal ID12985567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7044026..7159629hg38UCSC Ensembl
Innerchr3:7085713..7201316hg19UCSC Ensembl
Innerchr3:7060713..7176316hg18UCSC Ensembl
Innerchr3:7060713..7176316hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38115604
hg19115604
hg18115604
hg17115604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6987932, essv6981255, essv6987931, essv6981256
SamplesBEC_374
Known GenesGRM7
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)esv2752015
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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