A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984930



Internal ID12637054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15604702..15784602hg38UCSC Ensembl
Innerchr9:15604700..15784600hg19UCSC Ensembl
Innerchr9:15594700..15774600hg18UCSC Ensembl
Innerchr9:15594700..15774600hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38179901
hg19179901
hg18179901
hg17179901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752286
Supporting Variants
SamplesSPC_194
Known GenesCCDC171
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984930
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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