A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034638



Internal ID19123860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186264231..186292323hg38UCSC Ensembl
Innerchr4:187185385..187213477hg19UCSC Ensembl
Innerchr4:187422379..187450471hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3828093
hg1928093
hg1828093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635631
Samples
Known GenesF11, F11-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034638
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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