A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576185



Internal ID16016908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82018191..82035336hg38UCSC Ensembl
Innerchr17:79976067..79993212hg19UCSC Ensembl
Innerchr17:77569356..77586501hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3817146
hg1917146
hg1817146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5800n54
Supporting Variantsnssv877119
Samples
Known GenesLRRC45, RAC3, STRA13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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