A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998393



Internal ID19157929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87094919..87578874hg38UCSC Ensembl
Innerchr2:87322042..87878393hg19UCSC Ensembl
Innerchr2:87175553..87659508hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38483956
hg19556352
hg18483956
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3891n100
Supporting Variantsnssv3582186
Samples
Known GenesLINC00152, MIR4771-1, MIR4771-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998393
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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