A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029158



Internal ID18771690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57793025..58432738hg38UCSC Ensembl
Innerchr6:58142069..58759016hg19UCSC Ensembl
Innerchr6:58250028..58866975hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg38639714
hg19616948
hg18616948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657539
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)nsv1029158
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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