A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989512



Internal ID12978714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1221290..1404922hg38UCSC Ensembl
Innerchr9:1221290..1404922hg19UCSC Ensembl
Innerchr9:1211290..1394922hg18UCSC Ensembl
Innerchr9:1211290..1394922hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38183633
hg19183633
hg18183633
hg17183633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34351
Supporting Variants
SamplesNA11882
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989512
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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