A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582337



Internal ID18880618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87146758..87919212hg38UCSC Ensembl
Innerchr2:87373881..88218731hg19UCSC Ensembl
Innerchr2:87227392..87999846hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38772455
hg19844851
hg18772455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006743
Supporting Variants
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2, MIR4771-1, MIR4771-2, 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)nssv3582337
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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