A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574167



Internal ID16361576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1052582..1053226hg38UCSC Ensembl
Innerchr17:955822..956466hg19UCSC Ensembl
Innerchr17:902572..903216hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38645
hg19645
hg18645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5411n54
Supporting Variantsnssv866334, nssv866332, nssv866333
Samples
Known GenesABR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574167
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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