A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641196



Internal ID18592791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143363774..143377777hg38UCSC Ensembl
Innerchr4:144284927..144298930hg19UCSC Ensembl
Innerchr4:144504377..144518380hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3814004
hg1914004
hg1814004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018566
Supporting Variants
Samples
Known GenesGAB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3641196
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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