A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019797



Internal ID19109015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57946158..58051308hg38UCSC Ensembl
Innerchr6:58272436..58377586hg19UCSC Ensembl
Innerchr6:58380395..58485545hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg38105151
hg19105151
hg18105151
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5978n100
Supporting Variantsnssv3657554, nssv3657553
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)nsv1019797
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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