A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001754



Internal ID19090971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87146758..87500481hg38UCSC Ensembl
Innerchr2:87373881..87800000hg19UCSC Ensembl
Innerchr2:87227392..87581115hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38353724
hg19426120
hg18353724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3891n100
Supporting Variantsnssv3582257
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)nsv1001754
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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