A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024486



Internal ID19113703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143002899..143025567hg38UCSC Ensembl
Innerchr6:143324036..143346704hg19UCSC Ensembl
Innerchr6:143365729..143388397hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3822669
hg1922669
hg1822669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654452
Samples
Known GenesLOC100507489
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024486
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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