A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020886



Internal ID19110104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171072677..171218947hg38UCSC Ensembl
Innerchr4:171993828..172140098hg19UCSC Ensembl
Innerchr4:172230403..172376673hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38146271
hg19146271
hg18146271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635395
Samples
Known GenesMIR6082
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020886
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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