A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061066



Internal ID19150285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36084283..36258784hg38UCSC Ensembl
Innerchr17:34411640..34586282hg19UCSC Ensembl
Innerchr17:31435753..31610395hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38174502
hg19174643
hg18174643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561125
Samples
Known GenesCCL3, CCL3L1, CCL3L3, CCL4, CCL4L1, CCL4L2, TBC1D3B, TBC1D3H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061066
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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