A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023960



Internal ID19113177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143920939..144021781hg38UCSC Ensembl
Innerchr4:144842092..144942934hg19UCSC Ensembl
Innerchr4:145061542..145162384hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38100843
hg19100843
hg18100843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5423n100
Supporting Variantsnssv3635154, nssv3635153, nssv3635152, nssv3635155
Samples
Known GenesGYPB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023960
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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