A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982683



Internal ID12975374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11600514..11701727hg38UCSC Ensembl
Innerchr9:11600514..11701727hg19UCSC Ensembl
Innerchr9:11590514..11691727hg18UCSC Ensembl
Innerchr9:11590514..11691727hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38101214
hg19101214
hg18101214
hg17101214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752278
Supporting Variants
SamplesBEC_579
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982683
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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