A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579178



Internal ID18530773
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 StatusS
Merged Variantsnsv1013135
Supporting Variants
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)nssv3579178
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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