A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152826



Internal ID15875165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114421377..114517952hg38UCSC Ensembl
Innerchr4:115342533..115439108hg19UCSC Ensembl
Innerchr4:115561982..115658557hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3896576
hg1996576
hg1896576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595205
Supporting Variants
SamplesHGDP00645
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152826
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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