A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017514



Internal ID19106731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61860268hg38UCSC Ensembl
Innerchr9:44727847..44996420hg19UCSC Ensembl
Innerchr9:44667843..44936416hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38340260
hg19268574
hg18268574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695568, nssv3695569, nssv3695567
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)nsv1017514
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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