A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022480



Internal ID19111698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39455352..39709461hg38UCSC Ensembl
Innerchr9:41600370..41854479hg19UCSC Ensembl
Innerchr9:41590370..41844479hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38254110
hg19254110
hg18254110
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690221, nssv3690220
Samples
Known GenesLOC653501
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022480
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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