A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574842



Internal ID16015565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36186979..36194525hg38UCSC Ensembl
Innerchr17:34602419..34609970hg19UCSC Ensembl
Innerchr17:31626532..31634083hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387547
hg197552
hg187552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5554n54
Supporting Variantsnssv870042, nssv870041, nssv870037, nssv870039, nssv870045, nssv870040, nssv870044, nssv870043, nssv870038
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574842
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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