A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664226



Internal ID18962507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134707122..134727631hg38UCSC Ensembl
Innerchr7:134391874..134412383hg19UCSC Ensembl
Innerchr7:134042414..134062923hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3820510
hg1920510
hg1820510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020581
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3664226
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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