A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985434



Internal ID12635598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22739747..23462392hg38UCSC Ensembl
Innerchr19:22922549..23645194hg19UCSC Ensembl
Innerchr19:22714389..23437034hg18UCSC Ensembl
Innerchr19:22714389..23437034hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38722646
hg19722646
hg18722646
hg17722646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34907
Supporting Variants
SamplesNA19144
Known GenesLOC100132815, ZNF724P, ZNF728, ZNF730, ZNF91, ZNF99
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985434
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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