A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032121



Internal ID19121343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182083542..182102600hg38UCSC Ensembl
Innerchr4:183004695..183023753hg19UCSC Ensembl
Innerchr4:183241689..183260747hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3819059
hg1919059
hg1819059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635600
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032121
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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