A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023063



Internal ID19112280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61698692hg38UCSC Ensembl
Innerchr9:44727847..44906530hg19UCSC Ensembl
Innerchr9:44667843..44846526hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38178684
hg19178684
hg18178684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7603n100
Supporting Variantsnssv3695562, nssv3695561, nssv3695559, nssv3695564, nssv3695565, nssv3761483, nssv3695563, nssv3695560, nssv3761484, nssv3695566
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)nsv1023063
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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