A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033168



Internal ID19122390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:133560250..133722836hg38UCSC Ensembl
Innerchr7:133245004..133407589hg19UCSC Ensembl
Innerchr7:132895544..133058129hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38162587
hg19162586
hg18162586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3751547
Samples
Known GenesEXOC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033168
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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