A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032469



Internal ID19121691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135621043..135650625hg38UCSC Ensembl
Innerchr7:135305791..135335373hg19UCSC Ensembl
Innerchr7:134956331..134985913hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3829583
hg1929583
hg1829583
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664230
Samples
Known GenesNUP205
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032469
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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