A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575635



Internal ID16363044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53970327..54121732hg38UCSC Ensembl
Innerchr17:52047688..52199093hg19UCSC Ensembl
Innerchr17:49402687..49554092hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38151406
hg19151406
hg18151406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv874015
Samples
Known GenesMIR548AJ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575635
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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