A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028271



Internal ID19117489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180403065..180505206hg38UCSC Ensembl
Innerchr4:181324218..181426359hg19UCSC Ensembl
Innerchr4:181561212..181663353hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38102142
hg19102142
hg18102142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635598
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)nsv1028271
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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