A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022738



Internal ID19111956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5298129..5411412hg38UCSC Ensembl
Innerchr6:5298362..5411645hg19UCSC Ensembl
Innerchr6:5243361..5356644hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38113284
hg19113284
hg18113284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654739
Samples
Known GenesFARS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022738
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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