A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989326



Internal ID12975520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248181657..248442658hg38UCSC Ensembl
Innerchr1:248344959..248605959hg19UCSC Ensembl
Innerchr1:246411582..246672582hg18UCSC Ensembl
Innerchr1:244671000..244932000hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38261002
hg19261001
hg18261001
hg17261001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750833
Supporting Variants
SamplesBEC_592
Known GenesOR14C36, OR2M3, OR2M4, OR2M7, OR2T1, OR2T12, OR2T33, OR2T4, OR2T6
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989326
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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