A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032007



Internal ID19121229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137031551..137237659hg38UCSC Ensembl
Innerchr4:137952705..138158813hg19UCSC Ensembl
Innerchr4:138172155..138378263hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38206109
hg19206109
hg18206109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641123
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)nsv1032007
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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