A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018369



Internal ID18760902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2944928..2961123hg38UCSC Ensembl
Innerchr6:2945162..2961357hg19UCSC Ensembl
Innerchr6:2890161..2906356hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3816196
hg1916196
hg1816196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654721
Samples
Known GenesSERPINB6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018369
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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