A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010884



Internal ID19100101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88833599..89201738hg38UCSC Ensembl
Innerchr2:89133112..89501226hg19UCSC Ensembl
Innerchr2:88914227..89282341hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38368140
hg19368115
hg18368115
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3932n100
Supporting Variantsnssv3728970, nssv3728969, nssv3728967, nssv3728971, nssv3728968, nssv3728972, nssv3728966
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)nsv1010884
Frequency
Sample Size11257
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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