A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026970



Internal ID18769501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186616264..186992197hg38UCSC Ensembl
Innerchr4:187537418..187913351hg19UCSC Ensembl
Innerchr4:187774412..188150345hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38375934
hg19375934
hg18375934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5495n100
Supporting Variantsnssv3635640
Samples
Known GenesFAT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026970
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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