A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013135



Internal ID18755666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32771489..32820562hg38UCSC Ensembl
Innerchr2:32996556..33045629hg19UCSC Ensembl
Innerchr2:32850060..32899133hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3849074
hg1949074
hg1849074
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3752n100
Supporting Variantsnssv3579178
Samples
Known GenesTTC27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013135
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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