A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062304



Internal ID18804835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36084283..36157706hg38UCSC Ensembl
Innerchr17:34411640..34485079hg19UCSC Ensembl
Innerchr17:31435753..31509192hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3873424
hg1973440
hg1873440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561124, nssv3561123, nssv3561122
Samples
Known GenesCCL3, CCL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062304
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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