A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031886



Internal ID19121108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156046811..156086049hg38UCSC Ensembl
Innerchr4:156967963..157007201hg19UCSC Ensembl
Innerchr4:157187413..157226651hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3839239
hg1939239
hg1839239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744271
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)nsv1031886
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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