A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989631



Internal ID12973804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28197102..28295902hg38UCSC Ensembl
Innerchr9:28197100..28295900hg19UCSC Ensembl
Innerchr9:28187100..28285900hg18UCSC Ensembl
Innerchr9:28187100..28285900hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3898801
hg1998801
hg1898801
hg1798801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752294
Supporting Variants
SamplesBEC_451
Known GenesLINGO2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989631
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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