A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986286



Internal ID12975664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1062218..1823898hg38UCSC Ensembl
Innerchr9:1062218..1823898hg19UCSC Ensembl
Innerchr9:1052218..1813898hg18UCSC Ensembl
Innerchr9:1052218..1813898hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38761681
hg19761681
hg18761681
hg17761681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752273
Supporting Variants
SamplesBEC_605
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986286
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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