A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061448



Internal ID18803979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36102943..36265379hg38UCSC Ensembl
Innerchr17:34430336..34629684hg19UCSC Ensembl
Innerchr17:31454449..31653797hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38162437
hg19199349
hg18199349
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561166, nssv3561151, nssv3561153, nssv3561152, nssv3720064, nssv3561165, nssv3561161, nssv3561156, nssv3561155, nssv3561158, nssv3561162, nssv3561150, nssv3561154, nssv3561167, nssv3561168, nssv3561163, nssv3561159, nssv3561149, nssv3561164, nssv3561160, nssv3561157
Samples
Known GenesCCL3L1, 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)nsv1061448
Frequency
Sample Size29084
Observed Gain20
Observed Loss1
Observed Complex0
Frequencyn/a


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