A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007128



Internal ID19096346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24620083..24663638hg38UCSC Ensembl
Innerchr4:24621706..24665261hg19UCSC Ensembl
Innerchr4:24230804..24274359hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3843556
hg1943556
hg1843556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620596
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)nsv1007128
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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