A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011499



Internal ID19100716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89933859..90282526hg38UCSC Ensembl
Innerchr2:89972669..90321385hg19UCSC Ensembl
Innerchr2:89609974..89958690hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38348668
hg19348717
hg18348717
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3977n100
Supporting Variantsnssv3580511, nssv3580515, nssv3580514, nssv3580513, nssv3580512, nssv3580510
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011499
Frequency
Sample Size11257
Observed Gain1
Observed Loss5
Observed Complex0
Frequencyn/a


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