A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580221



Internal ID18878502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:111270033..111430144hg38UCSC Ensembl
Innerchr2:112027610..112187721hg19UCSC Ensembl
Innerchr2:111744081..111904192hg18UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38160112
hg19160112
hg18160112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001733
Supporting Variants
Samples
Known GenesMIR4435-1, MIR4435-1HG, MIR4435-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580221
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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