A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000613



Internal ID18743144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10722139..11715358hg38UCSC Ensembl
Innerchr4:10723763..11716982hg19UCSC Ensembl
Innerchr4:10332861..11326080hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38993220
hg19993220
hg18993220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619747
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)nsv1000613
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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