A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984874



Internal ID12983635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102086163..102184163hg38UCSC Ensembl
Innerchr9:104848445..104946445hg19UCSC Ensembl
Innerchr9:103888266..103986266hg18UCSC Ensembl
Innerchr9:101928000..102026000hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3898001
hg1998001
hg1898001
hg1798001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752272
Supporting Variants
SamplesSPC_188
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984874
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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