A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982067



Internal ID12974380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17970861..18015555hg38UCSC Ensembl
Innerchr9:17970859..18015553hg19UCSC Ensembl
Innerchr9:17960859..18005553hg18UCSC Ensembl
Innerchr9:17960859..18005553hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3844695
hg1944695
hg1844695
hg1744695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752288
Supporting Variants
SamplesBEC_516
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982067
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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