A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662211



Internal ID18960492
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 StatusS
Merged Variantsnsv1018261
Supporting Variants
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)nssv3662211
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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