A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012406



Internal ID18754939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:89246630..90245636hg38UCSC Ensembl
Innerchr4:90167781..91166787hg19UCSC Ensembl
Innerchr4:90386804..91385810hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38999007
hg19999007
hg18999007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3742881
Samples
Known GenesCCSER1, GPRIN3, LOC644248, MMRN1, SNCA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012406
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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