A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656213



Internal ID18607808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:107248084..107321887hg38UCSC Ensembl
Innerchr7:106888529..106962332hg19UCSC Ensembl
Innerchr7:106675765..106749568hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3873804
hg1973804
hg1873804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015615
Supporting Variants
Samples
Known GenesCOG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3656213
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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