A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575768



Internal ID16363177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58128727..58141352hg38UCSC Ensembl
Innerchr17:56206088..56218713hg19UCSC Ensembl
Innerchr17:53561087..53573712hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3812626
hg1912626
hg1812626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5729n54
Supporting Variantsnssv875528
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575768
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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