A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989806



Internal ID12629761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65303823..65453037hg38UCSC Ensembl
Innerchr7:64768750..64917950hg19UCSC Ensembl
Innerchr7:64406185..64555385hg18UCSC Ensembl
Innerchr7:64212900..64362100hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38149215
hg19149201
hg18149201
hg17149201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752165
Supporting Variants
SamplesBEC_666
Known GenesZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989806
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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