A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989030



Internal ID12978715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1184213..1413700hg38UCSC Ensembl
Innerchr9:1184213..1413700hg19UCSC Ensembl
Innerchr9:1174213..1403700hg18UCSC Ensembl
Innerchr9:1174213..1403700hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38229488
hg19229488
hg18229488
hg17229488
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989030
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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