A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576186



Internal ID16016909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82024601..82036150hg38UCSC Ensembl
Innerchr17:79982477..79994026hg19UCSC Ensembl
Innerchr17:77575766..77587315hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3811550
hg1911550
hg1811550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877120
Samples
Known GenesDCXR, LRRC45, RAC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576186
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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