A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989805



Internal ID12629762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65263155..65344337hg38UCSC Ensembl
Innerchr7:64728050..64809250hg19UCSC Ensembl
Innerchr7:64365485..64446685hg18UCSC Ensembl
Innerchr7:64172200..64253400hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3881183
hg1981201
hg1881201
hg1781201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752165
Supporting Variants
SamplesBEC_666
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989805
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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