A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574112



Internal ID16361521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:948940..949043hg38UCSC Ensembl
Innerchr17:852180..852283hg19UCSC Ensembl
Innerchr17:798930..799033hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38104
hg19104
hg18104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866092, nssv866091
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574112
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer