A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032273



Internal ID19121495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61952728hg38UCSC Ensembl
Innerchr9:44727847..45088880hg19UCSC Ensembl
Innerchr9:44667843..45028876hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38432720
hg19361034
hg18361034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7604n100
Supporting Variantsnssv3695571, nssv3695570
Samples
Known GenesFAM27C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032273
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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