A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574360



Internal ID16361769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:11281840..11306634hg38UCSC Ensembl
Innerchr17:11185157..11209951hg19UCSC Ensembl
Innerchr17:11125882..11150676hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3824795
hg1924795
hg1824795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149696
SamplesNINDS_160
Known GenesSHISA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574360
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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