A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980401



Internal ID12631635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485653..69499585hg38UCSC Ensembl
Innerchr9:72100569..72114501hg19UCSC Ensembl
Innerchr9:71290389..71304321hg18UCSC Ensembl
Innerchr9:69330123..69344055hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3813933
hg1913933
hg1813933
hg1713933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34257
Supporting Variants
SamplesNA10831
Known GenesAPBA1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980401
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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