A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061952



Internal ID19151171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42790226..42870449hg38UCSC Ensembl
Innerchr19:43294378..43374601hg19UCSC Ensembl
Innerchr19:47986218..48066441hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3880224
hg1980224
hg1880224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3564n100
Supporting Variantsnssv3569013
Samples
Known GenesLOC100289650, PSG1, PSG10P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061952
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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