A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982682



Internal ID12975376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11600500..11701700hg38UCSC Ensembl
Innerchr9:11600500..11701700hg19UCSC Ensembl
Innerchr9:11590500..11691700hg18UCSC Ensembl
Innerchr9:11590500..11691700hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38101201
hg19101201
hg18101201
hg17101201
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)essv6982682
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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