A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574227



Internal ID16014950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:2924664..3036687hg38UCSC Ensembl
Innerchr17:2827958..2939981hg19UCSC Ensembl
Innerchr17:2774708..2886731hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38112024
hg19112024
hg18112024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866442
Samples
Known GenesRAP1GAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574227
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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