A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016288



Internal ID18758823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179729085..182726257hg38UCSC Ensembl
Innerchr4:180650238..183647410hg19UCSC Ensembl
Innerchr4:180887232..183884404hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg382997173
hg192997173
hg182997173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635565
Samples
Known GenesLINC00290, MGC45800, MIR1305, MIR548AB, TENM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016288
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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