A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008337



Internal ID19097555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121413177..121473964hg38UCSC Ensembl
Innerchr4:122334332..122395119hg19UCSC Ensembl
Innerchr4:122553782..122614569hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3860788
hg1960788
hg1860788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5379n100
Supporting Variantsnssv3639384, nssv3639382, nssv3639385, nssv3639383
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)nsv1008337
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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