A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027781



Internal ID18770312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:142022332..142385414hg38UCSC Ensembl
Innerchr4:142943485..143306567hg19UCSC Ensembl
Innerchr4:143162935..143526017hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38363083
hg19363083
hg18363083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641191
Samples
Known GenesINPP4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027781
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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