A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985628



Internal ID12625777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135267209..135442209hg38UCSC Ensembl
Innerchr9:138159055..138334055hg19UCSC Ensembl
Innerchr9:137298876..137473876hg18UCSC Ensembl
Innerchr9:135385000..135560000hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38175001
hg19175001
hg18175001
hg17175001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752282
Supporting Variants
SamplesBEC_311
Known GenesC9orf62
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985628
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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