A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016714



Internal ID19105931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61587880hg38UCSC Ensembl
Innerchr9:44727847..44795718hg19UCSC Ensembl
Innerchr9:44667843..44735714hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3867872
hg1967872
hg1867872
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691950, nssv3757601, nssv3691952, nssv3691946, nssv3691951, nssv3691948, nssv3691944, nssv3691949, nssv3691945, nssv3757603, nssv3757602, nssv3691947, nssv3691943
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)nsv1016714
Frequency
Sample Size11257
Observed Gain1
Observed Loss12
Observed Complex0
Frequencyn/a


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