A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033871



Internal ID18776404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186931664..187977783hg38UCSC Ensembl
Innerchr4:187852818..188898937hg19UCSC Ensembl
Innerchr4:188089812..189135931hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381046120
hg191046120
hg181046120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635643
Samples
Known GenesLOC339975
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033871
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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