A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011519



Internal ID18754053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:112808752..112859418hg38UCSC Ensembl
Innerchr1:113351374..113402040hg19UCSC Ensembl
Innerchr1:113152897..113203563hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3850667
hg1950667
hg1850667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv290n100
Supporting Variantsnssv3492043
Samples
Known GenesLOC100996702
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011519
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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