A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015676



Internal ID18758210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12276419..12540792hg38UCSC Ensembl
Innerchr5:12276531..12540904hg19UCSC Ensembl
Innerchr5:12329531..12593904hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38264374
hg19264374
hg18264374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638204
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015676
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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