A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015645



Internal ID19104863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19469848..19570511hg38UCSC Ensembl
Innerchr9:19469846..19570509hg19UCSC Ensembl
Innerchr9:19459846..19560509hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38100664
hg19100664
hg18100664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690690
Samples
Known GenesSLC24A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015645
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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