A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022211



Internal ID19111429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179219472..179295043hg38UCSC Ensembl
Innerchr4:180140626..180216197hg19UCSC Ensembl
Innerchr4:180377620..180453191hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3875572
hg1975572
hg1875572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5486n100
Supporting Variantsnssv3635562
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)nsv1022211
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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