A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000106



Internal ID19089323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16336568..16373541hg38UCSC Ensembl
Innerchr4:16338191..16375164hg19UCSC Ensembl
Innerchr4:15947289..15984262hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3836974
hg1936974
hg1836974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5147n100
Supporting Variantsnssv3619855, nssv3737701, nssv3619851, nssv3619856, nssv3619850, nssv3619854, nssv3619853, nssv3619857, nssv3619852, nssv3737700, nssv3619849
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)nsv1000106
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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