A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998526



Internal ID19158062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89374858..89958690hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg18583833
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3968n100
Supporting Variantsnssv3582642, nssv3582644, nssv3582651, nssv3582655, nssv3582645, nssv3582659, nssv3582649, nssv3582648, nssv3582641, nssv3582650, nssv3582643, nssv3582657, nssv3582652, nssv3582653, nssv3582640, nssv3582639, nssv3582646, nssv3582656, nssv3582654, nssv3582647, nssv3582658
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)nsv998526
Frequency
Sample Size11257
Observed Gain6
Observed Loss15
Observed Complex0
Frequencyn/a


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