A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737769



Internal ID19036050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28244867..28418051hg38UCSC Ensembl
Innerchr4:28246489..28419673hg19UCSC Ensembl
Innerchr4:27855587..28028771hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38173185
hg19173185
hg18173185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012210
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)nssv3737769
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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