A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3728784



Internal ID19027065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87259942..87725136hg38UCSC Ensembl
Innerchr2:87487065..88024655hg19UCSC Ensembl
Innerchr2:87340576..87805770hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38465195
hg19537591
hg18465195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011195
Supporting Variants
Samples
Known GenesLINC00152, MIR4435-1, 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)nssv3728784
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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