A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574168



Internal ID16361577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1052582..1053277hg38UCSC Ensembl
Innerchr17:955822..956517hg19UCSC Ensembl
Innerchr17:902572..903267hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38696
hg19696
hg18696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5411n54
Supporting Variantsnssv866335, nssv866336, nssv866337
Samples
Known GenesABR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574168
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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