A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983547



Internal ID12976472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7260390..7373870hg38UCSC Ensembl
Innerchr9:7260390..7373870hg19UCSC Ensembl
Innerchr9:7250390..7363870hg18UCSC Ensembl
Innerchr9:7250390..7363870hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38113481
hg19113481
hg18113481
hg17113481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752310
Supporting Variants
SamplesBEC_667
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983547
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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