A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015731



Internal ID19104949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132975997..133029993hg38UCSC Ensembl
Innerchr4:133897152..133951148hg19UCSC Ensembl
Innerchr4:134116602..134170598hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3853997
hg1953997
hg1853997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5395n100
Supporting Variantsnssv3639527, nssv3743108
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)nsv1015731
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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