A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016101



Internal ID19105319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61622401hg38UCSC Ensembl
Innerchr9:44727847..44830239hg19UCSC Ensembl
Innerchr9:44667843..44770235hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38102393
hg19102393
hg18102393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7600n100
Supporting Variantsnssv3692143, nssv3692144, nssv3692147, nssv3692146, nssv3692145, nssv3692142, nssv3692141
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)nsv1016101
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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