A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007063



Internal ID19096281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:125746712..125803688hg38UCSC Ensembl
Innerchr4:126667867..126724843hg19UCSC Ensembl
Innerchr4:126887317..126944293hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3856977
hg1956977
hg1856977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639417
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)nsv1007063
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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