A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022823



Internal ID19112041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143981173..144021781hg38UCSC Ensembl
Innerchr4:144902326..144942934hg19UCSC Ensembl
Innerchr4:145121776..145162384hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3840609
hg1940609
hg1840609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635247
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)nsv1022823
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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