A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016744



Internal ID18759279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:13621911..13663796hg38UCSC Ensembl
Innerchr6:13622143..13664028hg19UCSC Ensembl
Innerchr6:13730122..13772007hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3841886
hg1941886
hg1841886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654789
Samples
Known GenesRANBP9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016744
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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