A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002368



Internal ID15949638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:76043035..76053198hg38UCSC Ensembl
Innerchr4:76964188..76974351hg19UCSC Ensembl
Innerchr4:77183212..77193375hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3810164
hg1910164
hg1810164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594692
Supporting Variants
Samples
Known GenesART3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1002368
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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