A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582192



Internal ID18880473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87094919..87661069hg38UCSC Ensembl
Innerchr2:87322042..87960588hg19UCSC Ensembl
Innerchr2:87175553..87741703hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38566151
hg19638547
hg18566151
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007588
Supporting Variants
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2, 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)nssv3582192
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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