A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985438



Internal ID12635612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22808784..23473618hg38UCSC Ensembl
Innerchr19:22991586..23656420hg19UCSC Ensembl
Innerchr19:22783426..23448260hg18UCSC Ensembl
Innerchr19:22783426..23448260hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38664835
hg19664835
hg18664835
hg17664835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34470
Supporting Variants
SamplesNA19145
Known GenesLOC100132815, ZNF724P, ZNF728, ZNF730, ZNF91
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985438
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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