A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527970



Internal ID15108577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87980166..87982720hg38UCSC Ensembl
Innerchr15:88523397..88525951hg19UCSC Ensembl
Innerchr15:86324401..86326955hg18UCSC Ensembl
Innerchr15:86324401..86326955hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg382555
hg192555
hg182555
hg172555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704482
Samples
Known GenesNTRK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527970
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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