A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999310



Internal ID19158846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:170096802..170254209hg38UCSC Ensembl
Innerchr1:170065943..170223350hg19UCSC Ensembl
Innerchr1:168332567..168489974hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38157408
hg19157408
hg18157408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3500071
Samples
Known GenesMETTL11B, MIR3119-1, MIR3119-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999310
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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