A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34907



Internal ID12644257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22739747..23500295hg38UCSC Ensembl
Innerchr19:22922549..23683097hg19UCSC Ensembl
Innerchr19:22714389..23474937hg18UCSC Ensembl
Innerchr19:22714389..23474937hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38760549
hg19760549
hg18760549
hg17760549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv138e55
Supporting Variantsessv6985434, essv6980921, essv6980923, essv6980922, essv6985435
SamplesNA19144
Known GenesLOC100132815, ZNF724P, ZNF728, ZNF730, ZNF91, ZNF99
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34907
Frequency
Sample Size771
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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