A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018128



Internal ID19107345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:136894492..137270858hg38UCSC Ensembl
Innerchr4:137815646..138192012hg19UCSC Ensembl
Innerchr4:138035096..138411462hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38376367
hg19376367
hg18376367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641121
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)nsv1018128
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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