A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007804



Internal ID19097023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:90201247..90296180hg38UCSC Ensembl
Innerchr4:91122398..91217331hg19UCSC Ensembl
Innerchr4:91341421..91436354hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3894934
hg1994934
hg1894934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3742885
Samples
Known GenesCCSER1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007804
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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