A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006086



Internal ID19095304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76804037..76901525hg38UCSC Ensembl
Innerchr2:77031163..77128651hg19UCSC Ensembl
Innerchr2:76884671..76982159hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3897489
hg1997489
hg1897489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3878n100
Supporting Variantsnssv3582052
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)nsv1006086
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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