A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1003648



Internal ID16297604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:103607152..103656225hg38UCSC Ensembl
Innerchr4:104528309..104577382hg19UCSC Ensembl
Innerchr4:104747758..104796831hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3849074
hg1949074
hg1849074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594985
Supporting Variants
Samples
Known GenesTACR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1003648
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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