A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988160



Internal ID12980049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22628701..22683801hg38UCSC Ensembl
Innerchr9:22628700..22683800hg19UCSC Ensembl
Innerchr9:22618700..22673800hg18UCSC Ensembl
Innerchr9:22618700..22673800hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3855101
hg1955101
hg1855101
hg1755101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34240
Supporting Variants
SamplesNA18532
Known GenesFLJ35282
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988160
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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