A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3615224



Internal ID18913505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:13278..51612hg38UCSC Ensembl
Innerchr4:13278..51506hg19UCSC Ensembl
Innerchr4:3278..41506hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3838335
hg1938229
hg1838229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014360
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3615224
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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