A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035019



Internal ID19124238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61665362hg38UCSC Ensembl
Innerchr9:44727847..44873200hg19UCSC Ensembl
Innerchr9:44667843..44813196hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38145354
hg19145354
hg18145354
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7602n100
Supporting Variantsnssv3695464, nssv3761470, nssv3761466, nssv3695462, nssv3761469, nssv3761468, nssv3695467, nssv3695463, nssv3695465, nssv3761467, nssv3695466, nssv3695468
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)nsv1035019
Frequency
Sample Size11257
Observed Gain6
Observed Loss6
Observed Complex0
Frequencyn/a


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