A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984156



Internal ID12977763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95439338..95441477hg38UCSC Ensembl
Innerchr8:96451566..96453705hg19UCSC Ensembl
Innerchr8:96520742..96522881hg18UCSC Ensembl
Innerchr8:96520742..96522881hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382140
hg192140
hg182140
hg172140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752270
Supporting Variants
SamplesBEC_789
Known GenesLOC100616530
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984156
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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