A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654218



Internal ID18605813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:116066..199503hg38UCSC Ensembl
Innerchr7:116066..199503hg19UCSC Ensembl
Innerchr7:211149..294586hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3883438
hg1983438
hg1883438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017321
Supporting Variants
Samples
Known GenesFAM20C, LOC100507642
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3654218
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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