A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017058



Internal ID18759593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57839293..58448438hg38UCSC Ensembl
Innerchr6:58165571..58774716hg19UCSC Ensembl
Innerchr6:58273530..58882675hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg38609146
hg19609146
hg18609146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5975n100
Supporting Variantsnssv3657540
Samples
Known GenesGUSBP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017058
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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