A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018041



Internal ID18760574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10465938..10530759hg38UCSC Ensembl
Innerchr6:10466171..10530992hg19UCSC Ensembl
Innerchr6:10574157..10638978hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3864822
hg1964822
hg1864822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5917n100
Supporting Variantsnssv3749020, nssv3654765
Samples
Known GenesGCNT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018041
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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