A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34384



Internal ID12990423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36643166..36839711hg38UCSC Ensembl
Innerchr19:37134068..37330613hg19UCSC Ensembl
Innerchr19:41825908..42022453hg18UCSC Ensembl
Innerchr19:41825908..42022453hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38196546
hg19196546
hg18196546
hg17196546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6979102, essv6979101
SamplesNA12891
Known GenesZNF461, ZNF567, ZNF790, ZNF790-AS1, ZNF850
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)esv34384
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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