A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032029



Internal ID18774563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152166450..152408521hg38UCSC Ensembl
Innerchr6:152487585..152729656hg19UCSC Ensembl
Innerchr6:152529278..152771349hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38242072
hg19242072
hg18242072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654474
Samples
Known GenesSYNE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032029
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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