A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3728001



Internal ID18679596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32621236..32791665hg38UCSC Ensembl
Innerchr2:32846303..33016732hg19UCSC Ensembl
Innerchr2:32699807..32870236hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38170430
hg19170430
hg18170430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005305
Supporting Variants
Samples
Known GenesMIR4765, TTC27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3728001
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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