A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616098



Internal ID18914379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:776106..1111676hg38UCSC Ensembl
Innerchr4:769894..1105464hg19UCSC Ensembl
Innerchr4:759894..1095464hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38335571
hg19335571
hg18335571
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003219
Supporting Variants
Samples
Known GenesCPLX1, DGKQ, FGFRL1, GAK, IDUA, LOC100129917, RNF212, SLC26A1, TMEM175
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616098
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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