A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3619757



Internal ID18571352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11586127..13990352hg38UCSC Ensembl
Innerchr4:11587751..13991976hg19UCSC Ensembl
Innerchr4:11196849..13601074hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382404226
hg192404226
hg182404226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014473
Supporting Variants
Samples
Known GenesBOD1L1, LINC01096, LINC01097, MIR5091, NKX3-2, RAB28
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3619757
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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