A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695571



Internal ID18647166
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 StatusS
Merged Variantsnsv1032273
Supporting Variants
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)nssv3695571
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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