A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010891



Internal ID18753424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11356827..12706554hg38UCSC Ensembl
Innerchr4:11358451..12708178hg19UCSC Ensembl
Innerchr4:10967549..12317276hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381349728
hg191349728
hg181349728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619756
Samples
Known GenesHS3ST1, MIR572
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010891
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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