A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023213



Internal ID19112430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140473839..141601250hg38UCSC Ensembl
Innerchr6:140794976..141922387hg19UCSC Ensembl
Innerchr6:140836669..141964080hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381127412
hg191127412
hg181127412
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749547
Samples
Known GenesMIR4465
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023213
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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