A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005091



Internal ID19094308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76782382..76885277hg38UCSC Ensembl
Innerchr2:77009508..77112403hg19UCSC Ensembl
Innerchr2:76863016..76965911hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38102896
hg19102896
hg18102896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3878n100
Supporting Variantsnssv3582051
Samples
Known GenesLRRTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005091
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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