A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574855



Internal ID16015578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36191328..36195856hg38UCSC Ensembl
Innerchr17:34606777..34611298hg19UCSC Ensembl
Innerchr17:31630890..31635411hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384529
hg194522
hg184522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5557n54
Supporting Variantsnssv870070, nssv870071
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574855
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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