A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153590



Internal ID15875931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:117964026..117995849hg38UCSC Ensembl
Innerchr5:117299721..117331544hg19UCSC Ensembl
Innerchr5:117327620..117359443hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3831824
hg1931824
hg1831824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599492
Supporting Variants
SamplesHGDP00759
Known GenesLOC102467224
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153590
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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