A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153264



Internal ID15873244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180454477..180500068hg38UCSC Ensembl
Innerchr4:181375630..181421221hg19UCSC Ensembl
Innerchr4:181612624..181658215hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3845592
hg1945592
hg1845592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596292
Supporting Variants
SamplesHGDP00150
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153264
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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