A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009633



Internal ID18752164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77966419..78731082hg38UCSC Ensembl
Innerchr4:78887573..79652236hg19UCSC Ensembl
Innerchr4:79106597..79871260hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38764664
hg19764664
hg18764664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633879
Samples
Known GenesANXA3, FRAS1, LINC01094
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009633
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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