A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582411



Internal ID18880692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87256879..87861756hg38UCSC Ensembl
Innerchr2:87484002..88161275hg19UCSC Ensembl
Innerchr2:87337513..87942390hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38604878
hg19677274
hg18604878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010878
Supporting Variants
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2, PLGLB1, PLGLB2, RGPD1, RGPD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3582411
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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