A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981908



Internal ID12974122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158026492..158056078hg38UCSC Ensembl
Innerchr7:157819184..157848770hg19UCSC Ensembl
Innerchr7:157511945..157541531hg18UCSC Ensembl
Innerchr7:157318660..157348246hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3829587
hg1929587
hg1829587
hg1729587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752150
Supporting Variants
SamplesBEC_500
Known GenesPTPRN2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981908
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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