A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001893



Internal ID19091110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..36298hg38UCSC Ensembl
Innerchr4:12269..36298hg19UCSC Ensembl
Innerchr4:2269..26298hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3824030
hg1924030
hg1824030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3617053, nssv3617054
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)nsv1001893
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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