A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574779



Internal ID16015502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36181006..36208705hg38UCSC Ensembl
Innerchr17:34508382..34536107hg19UCSC Ensembl
Innerchr17:31532495..31560220hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3827700
hg1927726
hg1827726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5541n54
Supporting Variantsnssv869903, nssv869904
Samples
Known GenesCCL3L1, CCL3L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574779
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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