A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018261



Internal ID19107478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:133379438..133433852hg38UCSC Ensembl
Innerchr7:133064192..133118606hg19UCSC Ensembl
Innerchr7:132714732..132769146hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3854415
hg1954415
hg1854415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6622n100
Supporting Variantsnssv3751545, nssv3751544, nssv3662211, nssv3662210, nssv3662209, nssv3751546
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)nsv1018261
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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