A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639448



Internal ID18937729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130044759..130083542hg38UCSC Ensembl
Innerchr4:130965914..131004697hg19UCSC Ensembl
Innerchr4:131185364..131224147hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3838784
hg1938784
hg1838784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028045
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)nssv3639448
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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