A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034755



Internal ID18777288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18064320..18173781hg38UCSC Ensembl
Innerchr6:18064551..18174012hg19UCSC Ensembl
Innerchr6:18172530..18281991hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38109462
hg19109462
hg18109462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749039
Samples
Known GenesKDM1B, NHLRC1, TPMT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034755
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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