A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575105



Internal ID16015828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45510291..45519155hg38UCSC Ensembl
Innerchr17:43587657..43596521hg19UCSC Ensembl
Innerchr17:40943440..40952304hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg388865
hg198865
hg188865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5610n54
Supporting Variantsnssv872243
Samples
Known GenesLRRC37A4P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575105
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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