A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641191



Internal ID18592786
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 StatusS
Merged Variantsnsv1027781
Supporting Variants
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)nssv3641191
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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