A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002664



Internal ID19091881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:93124339..93186536hg38UCSC Ensembl
Innerchr4:94045490..94107687hg19UCSC Ensembl
Innerchr4:94264513..94326710hg18UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg3862198
hg1962198
hg1862198
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3630975
Samples
Known GenesGRID2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002664
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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