A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048977



Internal ID18791508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84149197..84815576hg38UCSC Ensembl
Innerchr9:86764112..87430491hg19UCSC Ensembl
Innerchr9:85953932..86620311hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38666380
hg19666380
hg18666380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697529
Samples
Known GenesNTRK2, SLC28A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048977
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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