A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575103



Internal ID16015826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45408425..45419688hg38UCSC Ensembl
Innerchr17:43485791..43497054hg19UCSC Ensembl
Innerchr17:40841574..40852837hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3811264
hg1911264
hg1811264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv872241
Samples
Known GenesARHGAP27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575103
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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