A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3728725



Internal ID18680320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87110834..87747090hg38UCSC Ensembl
Innerchr2:87337957..88046609hg19UCSC Ensembl
Innerchr2:87191468..87827724hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38636257
hg19708653
hg18636257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007823
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)nssv3728725
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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