A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979076



Internal ID12979596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20098791..20206191hg38UCSC Ensembl
Innerchr19:20209600..20317000hg19UCSC Ensembl
Innerchr19:20070600..20178000hg18UCSC Ensembl
Innerchr19:20070600..20178000hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38107401
hg19107401
hg18107401
hg17107401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34357
Supporting Variants
SamplesNA12875
Known GenesZNF486, ZNF90
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979076
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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