A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059497



Internal ID18802028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36102943..36157706hg38UCSC Ensembl
Innerchr17:34430336..34485079hg19UCSC Ensembl
Innerchr17:31454449..31509192hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3854764
hg1954744
hg1854744
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561135, nssv3561139, nssv3561137, nssv3561130, nssv3720062, nssv3561133, nssv3561138, nssv3561134, nssv3561132, nssv3561140, nssv3720061, nssv3720063, nssv3561136, nssv3561131
Samples
Known GenesCCL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059497
Frequency
Sample Size29084
Observed Gain13
Observed Loss1
Observed Complex0
Frequencyn/a


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